Uncovering the molecular pathogenesis of congenital hyperinsulinism by panel gene sequencing in 32 Chinese patients.

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Congenital Hyperinsulinism in china: a review of Chinese literature over the past 15 years

P2860

Q39166993-30272610-45EE-44B2-AB2A-23D83641FE37

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Uncovering the molecular pathogenesis of congenital hyperinsulinism by panel gene sequencing in 32 Chinese patients.

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Uncovering the molecular patho ...... encing in 32 Chinese patients.

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Uncovering the molecular patho ...... encing in 32 Chinese patients.

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Uncovering the molecular patho ...... encing in 32 Chinese patients.

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P1476

Uncovering the molecular patho ...... encing in 32 Chinese patients.

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Bi-Jun Sun

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Hui-Jun Wang

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Jin-Wen Ni

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Li-Yuan Hu

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Lin Yang

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Mei Mei

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Si-Min Ma

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Wen-Hao Zhou

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Zi-Chuan Fan

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P2860

Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy

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

Preoperative evaluation of infants with focal or diffuse congenital hyperinsulinism by intravenous acute insulin response tests and selective pancreatic arterial calcium stimulation

Mutations in the hepatocyte nuclear factor-4alpha gene in maturity-onset diabetes of the young (MODY1)

Dysregulation of insulin secretion in children with congenital hyperinsulinism due to sulfonylurea receptor mutations

Human non-synonymous SNPs: server and survey

Prediction of deleterious human alleles

ESEfinder: A web resource to identify exonic splicing enhancers

Mutations in UCP2 in congenital hyperinsulinism reveal a role for regulation of insulin secretion

Molecular and clinical analysis of Japanese patients with persistent congenital hyperinsulinism: predominance of paternally inherited monoallelic mutations in the KATP channel genes.

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526-536

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scholarly article

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10.1002/MGG3.162

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2015-06-29T00:00:00Z

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280971274

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26740944

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birth defect

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4694131

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Uncovering the molecular pathogenesis of congenital hyperinsulinism by panel gene sequencing in 32 Chinese patients.

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P2860

P2860

Uncovering the molecular pathogenesis of congenital hyperinsulinism by panel gene sequencing in 32 Chinese patients.

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type

label

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P921

P932