{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,27]],"date-time":"2026-02-27T21:22:49Z","timestamp":1772227369247,"version":"3.50.1"},"reference-count":43,"publisher":"Springer Science and Business Media LLC","issue":"4","license":[{"start":{"date-parts":[[1999,4,1]],"date-time":"1999-04-01T00:00:00Z","timestamp":922924800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.springernature.com\/gp\/researchers\/text-and-data-mining"},{"start":{"date-parts":[[1999,4,1]],"date-time":"1999-04-01T00:00:00Z","timestamp":922924800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/www.springernature.com\/gp\/researchers\/text-and-data-mining"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Neurochem Res"],"published-print":{"date-parts":[[1999,4]]},"DOI":"10.1023\/a:1023957110171","type":"journal-article","created":{"date-parts":[[2003,6,9]],"date-time":"2003-06-09T16:05:44Z","timestamp":1055174744000},"page":"581-586","source":"Crossref","is-referenced-by-count":41,"title":["Rhizomelic Chondrodysplasia Punctata, a Peroxisomal Biogenesis Disorder Caused by Defects in Pex7p, a Peroxisomal Protein Import Receptor: A Minireview"],"prefix":"10.1007","volume":"24","author":[{"given":"P. Edward","family":"Purdue","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Marek","family":"Skoneczny","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Xudong","family":"Yang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jing-Wei","family":"Zhang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Paul B.","family":"Lazarow","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"469753_CR1","doi-asserted-by":"crossref","first-page":"430","DOI":"10.1007\/BF00441734","volume":"144","author":"R.B. Schutgens","year":"1986","unstructured":"Schutgens, R.B., Heymans, H.S., Wanders, R.J., Van den Bosch, H. and Tager, J.M. 1986. Peroxisomal disorders: a newly recognized group of genetic diseases. Eur. J. Pediatr. 144:430-440.","journal-title":"Eur. J. Pediatr."},{"key":"469753_CR2","first-page":"2287","volume-title":"The Metabolic Basis of Inherited Disease","author":"P.B. Lazarow","year":"1995","unstructured":"Lazarow, P.B. and Moser, H.W. 1995. Disorders of peroxisome biogenesis. In: The Metabolic Basis of Inherited Disease, edited by Scriver, C.R., Beaudet, A.L., Sly, W.S. and Valle, D. New York: McGraw-Hill, p. 2287-2324."},{"key":"469753_CR3","doi-asserted-by":"crossref","first-page":"13","DOI":"10.1016\/S0022-3476(95)70250-4","volume":"127","author":"A.B. Moser","year":"1995","unstructured":"Moser, A.B., Rasmussen, M., Naidu, S., et al. 1995. Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups. J. Pediatr. 127:13-22.","journal-title":"J. Pediatr."},{"key":"469753_CR4","doi-asserted-by":"crossref","first-page":"1536","DOI":"10.1126\/science.3281254","volume":"239","author":"M.J. Santos","year":"1988","unstructured":"Santos, M.J., Imanaka, T., Shio, H., Small, G.M. and Lazarow, P.B. 1988. Peroxisomal membrane ghosts in Zellweger syndromeaberrant organelle assembly. Science 239:1536-1538.","journal-title":"Science"},{"key":"469753_CR5","doi-asserted-by":"crossref","first-page":"10502","DOI":"10.1016\/S0021-9258(19)81544-2","volume":"263","author":"M.J. Santos","year":"1988","unstructured":"Santos, M.J., Imanaka, T., Shio, H. and Lazarow, P.B. 1988. Peroxisomal integral membrane proteins in control and Zellweger fibroblasts. J. Biol. Chem. 263:10502-10509.","journal-title":"J. Biol. Chem."},{"issue":"Suppl.2","key":"469753_CR6","doi-asserted-by":"crossref","first-page":"329","DOI":"10.1007\/BF01799743","volume":"9","author":"H.S.A. Heymans","year":"1986","unstructured":"Heymans, H.S.A., Oorthuys, J.W.E., Nelck, G., Wanders, R.J.A., Dingemans, K.P. and Schutgens, R.B.H. 1986. Peroxisomal abnormalities in rhizomelic chondrodysplasia punctata. J. Inherited Metab. Dis. 9Suppl. 2:329-331.","journal-title":"J. Inherited Metab. Dis."},{"key":"469753_CR7","first-page":"187","volume":"313","author":"H.S. Heymans","year":"1985","unstructured":"Heymans, H.S., Oorthuys, J.W., Nelck, G., Wanders, R.J. and Schutgens, R.B. 1985. Rhizomelic chondrodysplasia punctata: another peroxisomal disorder letter. N. Engl. J. Med. 313:187-188.","journal-title":"N. Engl. J. Med."},{"key":"469753_CR8","doi-asserted-by":"crossref","first-page":"726","DOI":"10.1016\/S0022-3476(88)80689-9","volume":"112","author":"G. Hoefler","year":"1988","unstructured":"Hoefler, G., Hoefler, S., Watkins, P.A., et al. 1988. Biochemical abnormalities in rhizomelic chondrodysplasia punctata. J. Pediatr. 112:726-733.","journal-title":"J. Pediatr."},{"key":"469753_CR9","doi-asserted-by":"crossref","first-page":"126","DOI":"10.1172\/JCI114674","volume":"86","author":"J.C. Heikoop","year":"1990","unstructured":"Heikoop, J.C., van Roermund, C.W., Just, W.W., et al. 1990. Rhizomelic chondrodysplasia punctata. Deficiency of 3-oxoacyl-coenzyme A thiolase in peroxisomes and impaired processing of the enzyme. J. Clin. Invest. 86:126-130.","journal-title":"J. Clin. Invest."},{"key":"469753_CR10","doi-asserted-by":"crossref","first-page":"444","DOI":"10.1023\/A:1005379406639","volume":"20","author":"G.A. Jansen","year":"1997","unstructured":"Jansen, G.A., Mihalik, S.J., Watkins, P.A., et al. 1997. Phytanoyl-CoA hydroxylase is not only deficient in classical Refsum disease but also in rhizomelic chondrodysplasia punctata. J. Inherited Metab. Dis. 20:444-446.","journal-title":"J. Inherited Metab. Dis."},{"key":"469753_CR11","doi-asserted-by":"crossref","first-page":"309","DOI":"10.1023\/A:1005353129761","volume":"21","author":"R.J.A. Wanders","year":"1988","unstructured":"Wanders, R.J.A. and Romeijn, G.J. 1988. Cholesterol biosynthesis, peroxisomes and peroxisomal disorders: Mevalonate kinase is not only deficient in Zellweger syndrome but also in rhizomelic chondrodysplasia punctata. J. Inherited Metab. Dis. 21:309-312.","journal-title":"J. Inherited Metab. Dis."},{"key":"469753_CR12","doi-asserted-by":"crossref","first-page":"389","DOI":"10.1007\/BF02435984","volume":"15","author":"R.J. Wanders","year":"1992","unstructured":"Wanders, R.J., Schumacher, H., Heikoop, J., Schutgens, R.B. and Tager, J.M. 1992. Human dihydroxyacetonephosphate acyltransferase deficiency: a new peroxisomal disorder. J. Inherit. Metab. Dis. 15:389-391.","journal-title":"J. Inherit. Metab. Dis."},{"key":"469753_CR13","doi-asserted-by":"crossref","first-page":"315","DOI":"10.1007\/BF00711817","volume":"17","author":"R.J.A. Wanders","year":"1994","unstructured":"Wanders, R.J.A., Dekker, C., Hovarth, V.A.P., et al. 1994. Human alkyldihydroxyacetonephosphate synthase deficiency: A new peroxisomal disorder. Journal of Inherited Metabolic Disease 17:315-318.","journal-title":"Journal of Inherited Metabolic Disease"},{"key":"469753_CR14","doi-asserted-by":"crossref","first-page":"369","DOI":"10.1038\/ng0497-369","volume":"15","author":"N. Braverman","year":"1997","unstructured":"Braverman, N., Steel, G., Obie, C., et al. 1997. Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata. Nature Genet. 15:369-376.","journal-title":"Nature Genet."},{"key":"469753_CR15","doi-asserted-by":"crossref","first-page":"377","DOI":"10.1038\/ng0497-377","volume":"15","author":"A.M. Motley","year":"1997","unstructured":"Motley, A.M., Hettema, E.H., Hogenhout, E.M., et al. 1997. Rhizomelic chondrodysplasia punctata is a peroxisomal protein targeting disease caused by a non-functional PTS2 receptor. Nature Genet. 15:377-380.","journal-title":"Nature Genet."},{"key":"469753_CR16","doi-asserted-by":"crossref","first-page":"381","DOI":"10.1038\/ng0497-381","volume":"15","author":"P.E. Purdue","year":"1997","unstructured":"Purdue, P.E., Zhang, J.W., Skoneczny, M. and Lazarow, P.B. 1997. Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptor. Nature Genet. 15:381-384.","journal-title":"Nature Genet."},{"key":"469753_CR17","doi-asserted-by":"crossref","first-page":"400","DOI":"10.1016\/S0962-8924(97)01126-4","volume":"7","author":"R. Erdmann","year":"1997","unstructured":"Erdmann, R., Veenhuis, M. and Kunau, W.H. 1997. Peroxisomes: organelles at the crossroads. Trends. Cell. Biol. 7:400-407.","journal-title":"Trends. Cell. Biol."},{"key":"469753_CR18","doi-asserted-by":"crossref","first-page":"171","DOI":"10.1152\/physrev.1998.78.1.171","volume":"78","author":"S. Subramani","year":"1998","unstructured":"Subramani, S. 1998. Components involved in peroxisome import, biogenesis, proliferation, turnover, and movement. Physiol. Rev. 78:171-188.","journal-title":"Physiol. Rev."},{"key":"469753_CR19","doi-asserted-by":"crossref","first-page":"1045","DOI":"10.1002\/yea.320111106","volume":"11","author":"P.E. Purdue","year":"1995","unstructured":"Purdue, P.E. and Lazarow, P.B. 1995. Identification of peroxisomal membrane ghosts with an epitope-tagged integral membrane protein in yeast mutants lacking peroxisomes. Yeast 11:1045-1060.","journal-title":"Yeast"},{"key":"469753_CR20","doi-asserted-by":"crossref","first-page":"30065","DOI":"10.1016\/S0021-9258(18)43771-4","volume":"269","author":"P.E. Purdue","year":"1994","unstructured":"Purdue, P.E. and Lazarow, P.B. 1994. Peroxisomal biogenesis: multiple pathways of protein import. J. Biol. Chem. 269:30065-30068.","journal-title":"J. Biol. Chem."},{"key":"469753_CR21","doi-asserted-by":"crossref","first-page":"755","DOI":"10.1083\/jcb.125.4.755","volume":"125","author":"A. Motley","year":"1994","unstructured":"Motley, A., Hettema, E., Distel, B. and Tabak, H. 1994. Differential protein import deficiencies in human peroxisome assembly disorders. J. Cell. Biol. 125:755-767.","journal-title":"J. Cell. Biol."},{"key":"469753_CR22","doi-asserted-by":"crossref","first-page":"761","DOI":"10.1083\/jcb.121.4.761","volume":"121","author":"D. McCollum","year":"1993","unstructured":"McCollum, D., Monosov, E. and Subramani, S. 1993. The pas8 mutant of Pichia pastoris exhibits the peroxisomal protein import deficiencies of Zellweger syndrome cells\u2014The PAS8 protein binds to the COOH-terminal tripeptide peroxisomal targeting signal, and is a member of the TPR protein family. J. Cell. Biol. 121:761-774.","journal-title":"J. Cell. Biol."},{"key":"469753_CR23","doi-asserted-by":"crossref","first-page":"3627","DOI":"10.1002\/j.1460-2075.1995.tb00032.x","volume":"14","author":"S.R. Terlecky","year":"1995","unstructured":"Terlecky, S.R., Nuttley, W.M., McCollum, D., Sock, E. and Subramani, S. 1995. The Pichia pastoris peroxisomal protein PAS8p is the receptor for the C-terminal tripeptide peroxisomal targeting signal. EMBO J. 14:3627-3634.","journal-title":"EMBO J."},{"key":"469753_CR24","doi-asserted-by":"crossref","first-page":"11782","DOI":"10.1073\/pnas.90.24.11782","volume":"90","author":"I. Van Der Leij","year":"1993","unstructured":"Van Der Leij, I., Franse, M.M., Elgersma, Y., Distel, B. and Tabak, H.F. 1993. PAS10 is a tetratricopeptide-repeat protein that is essential for the import of most matrix proteins into peroxisomes of Saccharomyces cerevisiae. Proc. Natl. Acad. Sci. USA 90:11782-11786.","journal-title":"Proc. Natl. Acad. Sci. USA"},{"key":"469753_CR25","doi-asserted-by":"crossref","first-page":"1453","DOI":"10.1083\/jcb.131.6.1453","volume":"131","author":"R.K. Szilard","year":"1995","unstructured":"Szilard, R.K., Titorenko, V.I., Veenhuis, M. and Rachubinski, R.A. 1995. Pay32p of the yeast Yarrowia lipolytica is an intraperoxisomal component of the matrix protein translocation machinery. J. Cell. Biol. 131:1453-1469.","journal-title":"J. Cell. Biol."},{"key":"469753_CR26","doi-asserted-by":"crossref","first-page":"17229","DOI":"10.1074\/jbc.270.29.17229","volume":"270","author":"I.J. van der Klei","year":"1995","unstructured":"van der Klei, I.J., Hilbrands, R.E., Swaving, G.J., et al. 1995. The Hansenula polymorpha PER3 gene is essential for the import of PTS1 proteins into the peroxisomal matrix. J. Biol. Chem. 270:17229-17236.","journal-title":"J. Biol. Chem."},{"key":"469753_CR27","doi-asserted-by":"crossref","first-page":"115","DOI":"10.1038\/ng0295-115","volume":"9","author":"G. Dodt","year":"1995","unstructured":"Dodt, G., Braverman, N., Wong, C., et al. 1995. Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders. Nature Genetics 9:115-125.","journal-title":"Nature Genetics"},{"key":"469753_CR28","doi-asserted-by":"crossref","first-page":"65","DOI":"10.1083\/jcb.129.1.65","volume":"129","author":"J.W. Zhang","year":"1994","unstructured":"Zhang, J.W. and Lazarow, P.B. 1994. PEBI (PAS7) in Saccharomyces cerevisiae encodes a hydrophilic, intraperoxisomal protein which is a member of the WD repeat family and is essential for the import of thiolase into peroxisomes. J. Cell. Biol. 129:65-80.","journal-title":"J. Cell. Biol."},{"key":"469753_CR29","doi-asserted-by":"crossref","first-page":"325","DOI":"10.1083\/jcb.132.3.325","volume":"132","author":"J.W. Zhang","year":"1996","unstructured":"Zhang, J.W. and Lazarow, P.B. 1996. Peblp (Pas7p) Is an Intraperoxisomal Receptor for the NH2-terminal, Type 2, Peroxisomal Targeting Sequence of Thiolase: Peb1p Itself Is Targeted to Peroxisomes by an NH2-terminal Peptide. J. Cell. Biol. 132:325-334.","journal-title":"J. Cell. Biol."},{"key":"469753_CR30","doi-asserted-by":"crossref","first-page":"4908","DOI":"10.1002\/j.1460-2075.1994.tb06818.x","volume":"13","author":"M. Marzioch","year":"1994","unstructured":"Marzioch, M., Erdmann, R., Veenhuis, M. and Kunau, W.-H. 1994. PAS7 encodes a novel yeast member of the WD-40 protein family essential for import of 3-oxoacyl-CoA thiolase, a PTS2-containing protein, into peroxisomes. EMBO J. 13:4908-4917.","journal-title":"EMBO J."},{"key":"469753_CR31","doi-asserted-by":"crossref","first-page":"3255","DOI":"10.1002\/j.1460-2075.1991.tb04889.x","volume":"10","author":"B.W. Swinkels","year":"1991","unstructured":"Swinkels, B.W., Gould, S.J., Bodnar, A.G., Rachubinski, R.A. and Subramani, S. 1991. A novel, cleavable peroxisomal targeting signal at the amino-terminus of the rat 3-ketoacyl-CoA thiolase. EMBO J. 10:3255-3262.","journal-title":"EMBO J."},{"key":"469753_CR32","doi-asserted-by":"crossref","first-page":"947","DOI":"10.1016\/0006-291X(91)92028-I","volume":"181","author":"T. Osumi","year":"1991","unstructured":"Osumi, T., Tsukamoto, T., Hata, S., et al. 1991. Amino-terminal presequence of the precursor of peroxisomal 3-ketoacyl-CoA thiolase is a cleavable signal peptide for peroxisomal targeting. Biochem. Biophys. Res. Commun. 181:947-954.","journal-title":"Biochem. Biophys. Res. Commun."},{"key":"469753_CR33","doi-asserted-by":"crossref","first-page":"7558","DOI":"10.1016\/S0021-9258(17)37323-4","volume":"269","author":"J.R. Glover","year":"1994","unstructured":"Glover, J.R., Andrews, D.W., Subramani, S. and Rachubinski, R.A. 1994. Mutagenesis of the amino targeting signal of Saccharomyces cerevisiae 3-ketoacyl-CoA thiolase reveals conserved amino acids required for import into peroxisomes in vivo. J. Biol. Chem. 269:7558-7563.","journal-title":"J. Biol. Chem."},{"key":"469753_CR34","doi-asserted-by":"crossref","first-page":"935","DOI":"10.1002\/yea.320100708","volume":"10","author":"R. Erdmann","year":"1994","unstructured":"Erdmann, R. 1994. The peroxisomal targeting signal of 3-oxoacyl-CoA thiolase from Saccharomyces cerevisiae. Yeast 10:935-944.","journal-title":"Yeast"},{"key":"469753_CR35","doi-asserted-by":"crossref","first-page":"306","DOI":"10.1023\/A:1005301112923","volume":"21","author":"P. Brites","year":"1998","unstructured":"Brites, P., Motley, A., Hogenhout, E., et al. 1998. Molecular basis of rhizomelic chondrodysplasia punctata type I: High frequency of the Leu-292 stop mutation in 38 patients. J. Inherited Metab. Dis. 21:306-308.","journal-title":"J. Inherited Metab. Dis."},{"key":"469753_CR36","doi-asserted-by":"crossref","first-page":"807","DOI":"10.1083\/jcb.140.4.807","volume":"140","author":"Y. Elgersma","year":"1998","unstructured":"Elgersma, Y., Elgersma-Hooisma, M., Wenzel, T., McCaffery, J.M., Farquhar, M.G. and Subramani, S. 1998. A mobile PTS2 receptor for peroxisomal protein import in Pichia pastoris. J. Cell. Biol. 140:807-820.","journal-title":"J. Cell. Biol."},{"key":"469753_CR37","doi-asserted-by":"crossref","first-page":"185","DOI":"10.1038\/ng1097-185","volume":"17","author":"S.J. Mihalik","year":"1997","unstructured":"Mihalik, S.J., Morrell, J.C., Kim, D., Sacksteder, K.A., Watkins, P.A. and Gould, S.J. 1997. Identification of PAHX,a Refsum disease gene. Nature Genet. 17:185-189.","journal-title":"Nature Genet."},{"key":"469753_CR38","doi-asserted-by":"crossref","first-page":"190","DOI":"10.1038\/ng1097-190","volume":"17","author":"G.A. Jansen","year":"1997","unstructured":"Jansen, G.A., Ferdinandusse, S., Ijlst, L., et al. 1997. Refsum disease is caused by mutations in the phytanoyl-CoA hydroxylase gene. Nature Genet. 17:190-193.","journal-title":"Nature Genet."},{"key":"469753_CR39","doi-asserted-by":"crossref","first-page":"25","DOI":"10.1016\/S0005-2760(97)00014-3","volume":"1346","author":"E.C.J.M. De Vet","year":"1997","unstructured":"De Vet, E.C.J.M., Van den Broek, B.T.E. and Van den Bosch, H. 1997. Nucleotide sequence of human alkyl-dihydroxyacetone-phosphate synthase cDNA reveals the presence of a peroxisomal targeting signal 2. Biochim. Biophys. Acta Lipids Lipid Metab. 1346:25-29.","journal-title":"Biochim. Biophys. Acta Lipids Lipid Metab."},{"key":"469753_CR40","doi-asserted-by":"crossref","first-page":"205","DOI":"10.1016\/S0014-5793(97)01495-6","volume":"420","author":"T.P. Thai","year":"1997","unstructured":"Thai, T.P., Heid, H., Rackwitz, H.R., Hunziker, A., Gorgas, K. and Just, W.W. 1997. Ether lipid biosynthesis: isolation and molecular characterization of human dihydroxyacetonephosphate acyltransferase. FEBS Lett. 420:205-211.","journal-title":"FEBS Lett."},{"key":"469753_CR41","doi-asserted-by":"crossref","first-page":"565","DOI":"10.1006\/bbrc.1997.7007","volume":"236","author":"R.J.A. Wanders","year":"1997","unstructured":"Wanders, R.J.A., Denis, S., Wouters, F., Wirtz, K.W.A. and Seedorf, U. 1997. Sterol carrier protein X (SCPx) is a peroxisomal branched-chain \u03b2-ketothiolase specifically reacting with 3-oxo-pristanoyl-CoA: A new, unique role for SCPx in branched-chain fatty acid metabolism in peroxisomes, Biochem. Biophys. Res. Commun. 236:565-569.","journal-title":"Biochem. Biophys. Res. Commun."},{"key":"469753_CR42","doi-asserted-by":"crossref","first-page":"2494","DOI":"10.1073\/pnas.84.8.2494","volume":"84","author":"A.W. Schram","year":"1987","unstructured":"Schram, A.W., Goldfischer, S., van Roermund, C.W.T., et al. 1987. Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency. Proc. Natl. Acad. Sci. USA 84:2494-2496.","journal-title":"Proc. Natl. Acad. Sci. USA"},{"key":"469753_CR43","doi-asserted-by":"crossref","first-page":"331","DOI":"10.1038\/ng0497-331","volume":"15","author":"S. Subramani","year":"1997","unstructured":"Subramani, S. 1997. PEX genes on the rise. Nature Genet. 15:331-333.","journal-title":"Nature Genet."}],"container-title":["Neurochemical Research"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/link.springer.com\/content\/pdf\/10.1023\/A:1023957110171.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/link.springer.com\/article\/10.1023\/A:1023957110171\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/link.springer.com\/content\/pdf\/10.1023\/A:1023957110171.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,6,12]],"date-time":"2025-06-12T09:19:26Z","timestamp":1749719966000},"score":1,"resource":{"primary":{"URL":"https:\/\/link.springer.com\/10.1023\/A:1023957110171"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1999,4]]},"references-count":43,"journal-issue":{"issue":"4","published-print":{"date-parts":[[1999,4]]}},"alternative-id":["469753"],"URL":"https:\/\/doi.org\/10.1023\/a:1023957110171","relation":{},"ISSN":["0364-3190","1573-6903"],"issn-type":[{"value":"0364-3190","type":"print"},{"value":"1573-6903","type":"electronic"}],"subject":[],"published":{"date-parts":[[1999,4]]}}}