Novel ABCC8 (SUR1) gene mutations in Asian Indian children with congenital hyperinsulinemic hypoglycemia.

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KCNJ11, ABCC8 and TCF7L2 polymorphisms and the response to sulfonylurea treatment in patients with type 2 diabetes: a bioinformatics assessment.

P2860

Q33771570-65D45489-5B23-415D-AE67-E197421439B8

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Novel ABCC8 (SUR1) gene mutations in Asian Indian children with congenital hyperinsulinemic hypoglycemia.

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http://www.wikidata.org/entity/Q46936149

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2014 nî lūn-bûn

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2014年の論文

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2014年学术文章

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name

Novel ABCC8 (SUR1) gene mutati ...... hyperinsulinemic hypoglycemia.

@en

Novel ABCC8

@nl

type

Item

label

Novel ABCC8 (SUR1) gene mutati ...... hyperinsulinemic hypoglycemia.

@en

Novel ABCC8

@nl

prefLabel

Novel ABCC8 (SUR1) gene mutati ...... hyperinsulinemic hypoglycemia.

@en

Novel ABCC8

@nl

P1476

Novel ABCC8 (SUR1) gene mutati ...... hyperinsulinemic hypoglycemia.

@en

P2093

Ashok Kumar Das

http://www.w3.org/2001/XMLSchema#string

Ayurchelvan Bhavatharini

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Dhanasekaran Bodhini

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Jaivinder Yadav

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Kandasamy Balamurugan

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Mahuya Sikdar

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Rajesh Khadgawat

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Sekar Kanthimathi

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Suresh Jahnavi

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Tanvir Kaur

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P2860

Reconstitution of IKATP: an inward rectifier subunit plus the sulfonylurea receptor

Permanent neonatal diabetes caused by dominant, recessive, or compound heterozygous SUR1 mutations with opposite functional effects.

Macrosomia and hyperinsulinaemic hypoglycaemia in patients with heterozygous mutations in the HNF4A gene

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

ATP-sensitive potassium channelopathies: focus on insulin secretion

Clinical and molecular genetics of neonatal diabetes due to mutations in the insulin gene.

Familial hyperinsulinemic hypoglycemia caused by a defect in the SCHAD enzyme of mitochondrial fatty acid oxidation.

Mutations in the sulonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews.

K(ATP) channels and insulin secretion disorders.

N-terminal transmembrane domain of the SUR controls trafficking and gating of Kir6 channel subunits.

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311-319

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scholarly article

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10.1111/AHG.12070

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English

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http://www.w3.org/2001/XMLSchema#string

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http://www.w3.org/2001/XMLSchema#string

P50

Viswanathan Mohan

P577

2014-09-01T00:00:00Z

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P5875

264743897

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P698

25117148

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P921

hypoglycemia

Novel ABCC8 (SUR1) gene mutations in Asian Indian children with congenital hyperinsulinemic hypoglycemia.

about

P2860

P2860

Novel ABCC8 (SUR1) gene mutations in Asian Indian children with congenital hyperinsulinemic hypoglycemia.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P5875

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P5875

P698

P921