{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,31]],"date-time":"2026-03-31T15:50:09Z","timestamp":1774972209028,"version":"3.50.1"},"reference-count":24,"publisher":"Elsevier BV","issue":"6","license":[{"start":{"date-parts":[[2002,12,1]],"date-time":"2002-12-01T00:00:00Z","timestamp":1038700800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Journal of American Association for Pediatric Ophthalmology and Strabismus"],"published-print":{"date-parts":[[2002,12]]},"DOI":"10.1067\/mpa.2002.129047","type":"journal-article","created":{"date-parts":[[2003,2,17]],"date-time":"2003-02-17T22:37:05Z","timestamp":1045521425000},"page":"393-396","source":"Crossref","is-referenced-by-count":13,"title":["Grating acuity in albinism in the first three years of life"],"prefix":"10.1067","volume":"6","author":[{"given":"Sarah J.","family":"Whang","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Richard A.","family":"King","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C.Gail","family":"Summers","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1067\/mpa.2002.129047_bib1","first-page":"1095","article-title":"Vision in albinism","volume":"94","author":"Summers","year":"1996","journal-title":"Trans Am Ophthalmol Soc"},{"key":"10.1067\/mpa.2002.129047_bib2","doi-asserted-by":"crossref","first-page":"337","DOI":"10.1007\/BF00155678","article-title":"Visual acuity development in tyrosinase negative oculocutaneous albinism","volume":"56","author":"Jacobson","year":"1984","journal-title":"Doc Opthalmol"},{"key":"10.1067\/mpa.2002.129047_bib3","first-page":"653","article-title":"Delayed visual maturation","volume":"104","author":"Fielder","year":"1985","journal-title":"Trans Ophthalmol Soc UK"},{"key":"10.1067\/mpa.2002.129047_bib4","doi-asserted-by":"crossref","first-page":"101","DOI":"10.3109\/13816819209087610","article-title":"Preferential looking: clinical lessons","volume":"13","author":"Fielder","year":"1992","journal-title":"Ophthalmic Paediatr Genet"},{"key":"10.1067\/mpa.2002.129047_bib5","doi-asserted-by":"crossref","first-page":"545","DOI":"10.1016\/S0161-6420(88)33152-0","article-title":"Hermansky-Pudlak syndrome: ophthalmic findings","volume":"95","author":"Summers","year":"1988","journal-title":"Ophthalmology"},{"key":"10.1067\/mpa.2002.129047_bib6","first-page":"657","article-title":"Large sample population age norms for visual acuities obtained with Vistech\u2014Teller acuity cards","volume":"36","author":"Salam\u00e3o","year":"1995","journal-title":"Invest Ophthalmol Vis Sci"},{"key":"10.1067\/mpa.2002.129047_bib7","first-page":"191","article-title":"Statistical methods","author":"Snedecor","year":"1980"},{"key":"10.1067\/mpa.2002.129047_bib8","doi-asserted-by":"crossref","first-page":"1724","DOI":"10.1056\/NEJM199006143222407","article-title":"Detection of mutations in the tyrosinase gene in a patient with Type 1A oculocutaneous albinism","volume":"322","author":"Pritz","year":"1990","journal-title":"N Engl J Med"},{"key":"10.1067\/mpa.2002.129047_bib9","doi-asserted-by":"crossref","first-page":"990","DOI":"10.1016\/0006-291X(89)91767-1","article-title":"Human oculocutaneous albinism caused by a single base insertion in the tyrosinase gene","volume":"164","author":"Tomita","year":"1989","journal-title":"Biochem Biophys Res Commun"},{"key":"10.1067\/mpa.2002.129047_bib10","doi-asserted-by":"crossref","first-page":"1121","DOI":"10.1126\/science.257.5073.1121","article-title":"The mouse pink-eyed dilution gene: association with human Prader-Willi and Angelman syndromes","volume":"257","author":"Gardner","year":"1992","journal-title":"Science"},{"key":"10.1067\/mpa.2002.129047_bib11","doi-asserted-by":"crossref","first-page":"72","DOI":"10.1038\/361072a0","article-title":"A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism","volume":"361","author":"Rinchik","year":"1993","journal-title":"Nature"},{"key":"10.1067\/mpa.2002.129047_bib12","first-page":"1145","article-title":"Mutation in and lack of expression of tyrosinase-related protein-1 (TRP-1) in melanocytes from an individual with brown oculocutaneous albinism: a new subtype of albinism classified as \u201cOCA3\u201d","volume":"48","author":"Boissy","year":"1996","journal-title":"Am J Hum Genet"},{"key":"10.1067\/mpa.2002.129047_bib13","doi-asserted-by":"crossref","first-page":"981","DOI":"10.1086\/324340","article-title":"Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4","volume":"69","author":"Newton","year":"2001","journal-title":"Am J Hum Genet"},{"key":"10.1067\/mpa.2002.129047_bib14","doi-asserted-by":"crossref","first-page":"9238","DOI":"10.1073\/pnas.94.17.9238","article-title":"The mouse pale ear (ep) mutation is the homologue of human Hermansky-Pudlak syndrome","volume":"94","author":"Gardner","year":"1997","journal-title":"Proc Natl Acad Sci USA"},{"key":"10.1067\/mpa.2002.129047_bib15","doi-asserted-by":"crossref","first-page":"300","DOI":"10.1038\/ng1196-300","article-title":"Positional cloning of a gene for Hermansky-Pudlak syndrome, a disorder of cytoplasmic organelles","volume":"14","author":"Oh","year":"1996","journal-title":"Nat Genet"},{"key":"10.1067\/mpa.2002.129047_bib16","doi-asserted-by":"crossref","first-page":"423","DOI":"10.1016\/S0002-9343(99)00436-2","article-title":"A new variant of Hermansky-Pudlak syndrome due to mutations in a gene responsible for vesicle formation","volume":"108","author":"Shotelersuk","year":"2000","journal-title":"Am J Med"},{"key":"10.1067\/mpa.2002.129047_bib17","doi-asserted-by":"crossref","first-page":"1022","DOI":"10.1086\/324168","article-title":"Hermansky-Pudlak syndrome type 3 in Ashkenazi Jews and other non-Puerto Rican patients with hypopigmentation and platelet storage-pool deficiency","volume":"69","author":"Huizing","year":"2001","journal-title":"Am J Hum Genet"},{"key":"10.1067\/mpa.2002.129047_bib18","doi-asserted-by":"crossref","first-page":"321","DOI":"10.1038\/ng835","article-title":"Hermansky-Pudlak syndrome is caused by mutations in HPS4, the human homolog of the mouse light-ear gene","volume":"30","author":"Suzuki","year":"2002","journal-title":"Nat Genet"},{"key":"10.1067\/mpa.2002.129047_bib19","doi-asserted-by":"crossref","first-page":"307","DOI":"10.1038\/ng1196-307","article-title":"Identification and mutation analysis of the complete gene for Chediak-Higashi syndrome","volume":"14","author":"Nagle","year":"1996","journal-title":"Nat Genet"},{"key":"10.1067\/mpa.2002.129047_bib20","doi-asserted-by":"crossref","first-page":"1091","DOI":"10.1093\/hmg\/6.7.1091","article-title":"Identification of mutations in two major mRNA isoforms of the Chediak-Higashi syndrome gene in human and mouse","volume":"6","author":"Barbosa","year":"1997","journal-title":"Hum Mol Genet"},{"key":"10.1067\/mpa.2002.129047_bib21","first-page":"1158","article-title":"The acuity card procedure: a rapid test of infant acuity","volume":"26","author":"McDonald","year":"1985","journal-title":"Invest Ophthalmol Vis Sci"},{"key":"10.1067\/mpa.2002.129047_bib22","doi-asserted-by":"crossref","first-page":"64","DOI":"10.3928\/0191-3913-19870301-04","article-title":"Operant acuity of toddlers and developmentally delayed children with low vision","volume":"24","author":"Birch","year":"1987","journal-title":"J Pediatr Ophthalmol Strabismus"},{"key":"10.1067\/mpa.2002.129047_bib23","doi-asserted-by":"crossref","first-page":"312","DOI":"10.3928\/0191-3913-19981101-05","article-title":"Assessing visual function in children younger than 1 1\/2 years with normal and subnormal vision: evaluation of methods","volume":"35","author":"Rydberg","year":"1998","journal-title":"J Pediatr Ophthalmol Strabismus"},{"key":"10.1067\/mpa.2002.129047_bib24","doi-asserted-by":"crossref","first-page":"259","DOI":"10.3928\/0191-3913-19930701-09","article-title":"The effect of grating orientation on resolution acuity in patients with nystagmus","volume":"30","author":"Meiusi","year":"1993","journal-title":"J Pediatr Ophthalmol Strabismus"}],"container-title":["Journal of American Association for Pediatric Ophthalmology and Strabismus"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1091853102000988?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1091853102000988?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2021,6,2]],"date-time":"2021-06-02T20:17:19Z","timestamp":1622665039000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1091853102000988"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2002,12]]},"references-count":24,"journal-issue":{"issue":"6","published-print":{"date-parts":[[2002,12]]}},"alternative-id":["S1091853102000988"],"URL":"https:\/\/doi.org\/10.1067\/mpa.2002.129047","relation":{},"ISSN":["1091-8531"],"issn-type":[{"value":"1091-8531","type":"print"}],"subject":[],"published":{"date-parts":[[2002,12]]}}}