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A new familial form of a late-onset, persistent hyperinsulinemic hypoglycemia of infancy caused by a novel mutation in KCNJ11.
Yang, Yen-Yu; Long, Roger K; Ferrara, Christine T; Gitelman, Stephen E; German, Michael S; Yang, Shi-Bing.
Affiliation
  • Yang YY; a Institute of Biomedical Sciences, Academia Sinica , Taipei , Taiwan.
  • Long RK; b Department of Pediatrics , University of California San Francisco , USA.
  • Ferrara CT; b Department of Pediatrics , University of California San Francisco , USA.
  • Gitelman SE; b Department of Pediatrics , University of California San Francisco , USA.
  • German MS; c Diabetes Center , University of California San Francisco , USA.
  • Yang SB; c Diabetes Center , University of California San Francisco , USA.
Channels (Austin) ; 11(6): 636-647, 2017 Nov 02.
Article in En | MEDLINE | ID: mdl-29087246
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Potassium Channels, Inwardly Rectifying / Congenital Hyperinsulinism / Mutation Limits: Humans Language: En Journal: Channels (Austin) Year: 2017 Document type: Article Affiliation country: Taiwán Country of publication: Estados Unidos
Fulltext
Add to My VHL
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Potassium Channels, Inwardly Rectifying / Congenital Hyperinsulinism / Mutation Limits: Humans Language: En Journal: Channels (Austin) Year: 2017 Document type: Article Affiliation country: Taiwán Country of publication: Estados Unidos