A new familial form of a late-onset, persistent hyperinsulinemic hypoglycemia of infancy caused by a novel mutation in KCNJ11-Reference-Cited by-同舟云学术

A new familial form of a late-onset, persistent hyperinsulinemic hypoglycemia of infancy caused by a novel mutation in KCNJ11

Published:2017-11-02 Issue:6 Volume:11 Page:636-647
ISSN:1933-6950
Container-title:Channels
language:en
Short-container-title:Channels

Author:

Yang Yen-Yu¹^ORCID,Long Roger K.²,Ferrara Christine T.²,Gitelman Stephen E.²³,German Michael S.³⁴,Yang Shi-Bing¹^ORCID

Affiliation:

1. Institute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan

2. Department of Pediatrics, University of California San Francisco, USA

3. Diabetes Center, University of California San Francisco, USA

4. Department of Medicine and Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California San Francisco, USA

Publisher

Informa UK Limited

Subject

Biochemistry,Biophysics

Link

https://www.tandfonline.com/doi/pdf/10.1080/19336950.2017.1393131

Reference47 articles.

1. Persistent hyperinsulinemic hypoglycemia of infancy: An overview of current concepts

2. Genotype and Phenotype Correlations in 417 Children With Congenital Hyperinsulinism

3. Clinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with dominant KATP channel mutations

4. Genotype-Phenotype Correlations in Children with Congenital Hyperinsulinism Due to Recessive Mutations of the Adenosine Triphosphate-Sensitive Potassium Channel Genes

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