{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,4,7]],"date-time":"2023-04-07T08:32:12Z","timestamp":1680856332041},"reference-count":26,"publisher":"Walter de Gruyter GmbH","issue":"5-6","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2013,1,1]]},"DOI":"10.1515\/jpem-2012-0133","type":"journal-article","created":{"date-parts":[[2013,5,2]],"date-time":"2013-05-02T22:41:06Z","timestamp":1367534466000},"source":"Crossref","is-referenced-by-count":3,"title":["KCNJ11 in-frame 15-bp deletion leading to glibenclamide- responsive neonatal diabetes mellitus in a Chinese child"],"prefix":"10.1515","volume":"26","author":[{"given":"Wenli","family":"Yang","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Huiqin","family":"Wei","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yanmei","family":"Sang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"374","reference":[{"key":"ref161","first-page":"101","article-title":"AT Molecular basis of Kir mutations associated with neonatal diabetes or neonatal diabetes plus neurological features","volume":"6","author":"Proks","year":"2004","journal-title":"Proc Natl Acad Sci USA"},{"key":"ref121","first-page":"355","article-title":"Switching from insulin to oral sulfonylureas in patients with diabetes due to Kir mutations","volume":"6","author":"Pearson","year":"2006","journal-title":"Engl J Med"},{"key":"ref231","first-page":"1","article-title":"An in - frame deletion in Kir causing neonatal diabetes reveals a site of interaction between Kir","volume":"6","author":"Craig","year":"2009","journal-title":"SUR J Clin Endocrinol Metab"},{"key":"ref281","doi-asserted-by":"crossref","first-page":"616","DOI":"10.3346\/jkms.2007.22.4.616","article-title":"Sulfonylurea therapy in two Korean patients with insulin - treated neonatal diabetes due to heterozygous mutations of the KCNJ gene encoding Kir","volume":"11","author":"Kim","year":"2007","journal-title":"J Korean Med Sci"},{"key":"ref101","doi-asserted-by":"crossref","first-page":"3979","DOI":"10.1210\/jc.2007-0486","article-title":"Molecular basis of neonatal diabetes in Japanese patients","author":"Suzuki","year":"2007","journal-title":"J Clin Endocrinol Metab"},{"key":"ref131","doi-asserted-by":"crossref","first-page":"616","DOI":"10.3346\/jkms.2007.22.4.616","article-title":"Sulfonylurea therapy in two Korean patients with insulin - treated neonatal diabetes due to heterozygous mutations of the KCNJ gene encoding Kir","volume":"11","author":"Kim","year":"2007","journal-title":"J Korean Med Sci"},{"key":"ref251","doi-asserted-by":"crossref","first-page":"3979","DOI":"10.1210\/jc.2007-0486","article-title":"Molecular basis of neonatal diabetes in Japanese patients","author":"Suzuki","year":"2007","journal-title":"J Clin Endocrinol Metab"},{"key":"ref181","first-page":"947","article-title":"Permanent neonatal diabetes due to gene mutation","volume":"11","author":"Letha","year":"2007","journal-title":"Paediatr"},{"key":"ref241","doi-asserted-by":"crossref","first-page":"824","DOI":"10.1038\/sj.ejhg.5201629","article-title":"activating mutations are associated with developmental delay epilepsy and neonatal diabetes syndrome and other neurological features","volume":"11","author":"Gloyn","year":"2006","journal-title":"Eur J Hum Genet"},{"key":"ref41","first-page":"1","article-title":"Kir mutations causing neonatal diabetes provide new insights into Kir interactions","volume":"6","author":"Tammaro","year":"2005","journal-title":"SUR EMBO J"},{"key":"ref31","first-page":"947","article-title":"Permanent neonatal diabetes due to gene mutation","volume":"11","author":"Letha","year":"2007","journal-title":"Paediatr"},{"key":"ref71","first-page":"1","article-title":"Insulin mutation screening in patients with diabetes : mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood","author":"Edghill","year":"2008","journal-title":"Diabetes"},{"key":"ref11","first-page":"101","article-title":"AT Molecular basis of Kir mutations associated with neonatal diabetes or neonatal diabetes plus neurological features","volume":"6","author":"Proks","year":"2004","journal-title":"Proc Natl Acad Sci USA"},{"key":"ref151","doi-asserted-by":"crossref","first-page":"645","DOI":"10.1016\/S0092-8674(00)80701-1","article-title":"Targeted overactivity of beta cell channels induces pro - found neonatal diabetes","author":"Koster","year":"2000","journal-title":"Cell"},{"key":"ref201","doi-asserted-by":"crossref","DOI":"10.2337\/db07-0043","article-title":"Mutations in ATP sensitive channel genes cause transient neonatal diabetes and permanent diabetes in childhood or adulthood","author":"Flanagan","year":"2007","journal-title":"Diabetes"},{"key":"ref21","first-page":"2503","article-title":"Hattersley AT Activating mutations in Kir neonatal diabetes : new clinical syndromes new scientific insights and new therapy","volume":"6","author":"Ashcroft","year":"2005","journal-title":"Diabetes"},{"key":"ref51","doi-asserted-by":"crossref","DOI":"10.2337\/db07-0043","article-title":"Mutations in ATP sensitive channel genes cause transient neonatal diabetes and permanent diabetes in childhood or adulthood","author":"Flanagan","year":"2007","journal-title":"Diabetes"},{"key":"ref111","first-page":"49","article-title":"AT Mutations in KCNJ which encodes Kir are a common cause of diabetes diagnosed in the first months of life with the phenotype determined by genotype","volume":"11","author":"Flanagan","year":"2006","journal-title":"Diabetologia"},{"key":"ref91","doi-asserted-by":"crossref","first-page":"824","DOI":"10.1038\/sj.ejhg.5201629","article-title":"activating mutations are associated with developmental delay epilepsy and neonatal diabetes syndrome and other neurological features","volume":"11","author":"Gloyn","year":"2006","journal-title":"Eur J Hum Genet"},{"key":"ref81","first-page":"1","article-title":"An in - frame deletion in Kir causing neonatal diabetes reveals a site of interaction between Kir","volume":"6","author":"Craig","year":"2009","journal-title":"SUR J Clin Endocrinol Metab"},{"key":"ref221","first-page":"1","article-title":"Insulin mutation screening in patients with diabetes : mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood","author":"Edghill","year":"2008","journal-title":"Diabetes"},{"key":"ref271","first-page":"355","article-title":"Switching from insulin to oral sulfonylureas in patients with diabetes due to Kir mutations","volume":"6","author":"Pearson","year":"2006","journal-title":"Engl J Med"},{"key":"ref261","first-page":"49","article-title":"AT Mutations in KCNJ which encodes Kir are a common cause of diabetes diagnosed in the first months of life with the phenotype determined by genotype","volume":"11","author":"Flanagan","year":"2006","journal-title":"Diabetologia"},{"key":"ref01","doi-asserted-by":"crossref","first-page":"645","DOI":"10.1016\/S0092-8674(00)80701-1","article-title":"Targeted overactivity of beta cell channels induces pro - found neonatal diabetes","author":"Koster","year":"2000","journal-title":"Cell"},{"key":"ref171","first-page":"2503","article-title":"Hattersley AT Activating mutations in Kir neonatal diabetes : new clinical syndromes new scientific insights and new therapy","volume":"6","author":"Ashcroft","year":"2005","journal-title":"Diabetes"},{"key":"ref191","first-page":"1","article-title":"Kir mutations causing neonatal diabetes provide new insights into Kir interactions","volume":"6","author":"Tammaro","year":"2005","journal-title":"SUR EMBO J"}],"container-title":["Journal of Pediatric Endocrinology and Metabolism"],"original-title":[],"link":[{"URL":"https:\/\/www.degruyter.com\/document\/doi\/10.1515\/jpem-2012-0133\/pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2021,4,22]],"date-time":"2021-04-22T01:33:31Z","timestamp":1619055211000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.degruyter.com\/document\/doi\/10.1515\/jpem-2012-0133\/html"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2013,1,1]]},"references-count":26,"journal-issue":{"issue":"5-6"},"URL":"https:\/\/doi.org\/10.1515\/jpem-2012-0133","relation":{},"ISSN":["2191-0251","0334-018X"],"issn-type":[{"value":"2191-0251","type":"electronic"},{"value":"0334-018X","type":"print"}],"subject":[],"published":{"date-parts":[[2013,1,1]]}}}