The Common p.R114W HNF4A Mutation Causes a Distinct Clinical Subtype of Monogenic Diabetes. - Wikidata - awgldk - TriplyDB

The Common p.R114W HNF4A Mutation Causes a Distinct Clinical Subtype of Monogenic Diabetes.

The Common p.R114W HNF4A Mutation Causes a Distinct Clinical Subtype of Monogenic Diabetes.

http://www.wikidata.org/entity/Q37281017

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Precision diabetes: learning from monogenic diabetes.Management of sulfonylurea-treated monogenic diabetes in pregnancy: implications of placental glibenclamide transfer.Spectrum of mutations in monogenic diabetes genes identified from high-throughput DNA sequencing of 6888 individuals.Use of oral antidiabetic drugs in the treatment of maturity-onset diabetes of the young: A mini review.Towards a systematic nationwide screening strategy for MODY.Loss-of-function mutations in Zn-finger DNA-binding domain of HNF4A cause aberrant transcriptional regulation in liver cancer.An Atypical HNF4A Mutation Which Does Not Conform to the Classic Presentation of HNF4A-MODY.

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The Common p.R114W HNF4A Mutation Causes a Distinct Clinical Subtype of Monogenic Diabetes.

http://www.wikidata.org/entity/Q37281017

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

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scientific article published on 02 August 2016

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

The Common p.R114W HNF4A Mutat ...... Subtype of Monogenic Diabetes.

@en

The Common p.R114W HNF4A Mutat ...... Subtype of Monogenic Diabetes.

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type

label

The Common p.R114W HNF4A Mutat ...... Subtype of Monogenic Diabetes.

@en

The Common p.R114W HNF4A Mutat ...... Subtype of Monogenic Diabetes.

@nl

prefLabel

The Common p.R114W HNF4A Mutat ...... Subtype of Monogenic Diabetes.

@en

The Common p.R114W HNF4A Mutat ...... Subtype of Monogenic Diabetes.

@nl

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The Common p.R114W HNF4A Mutat ...... Subtype of Monogenic Diabetes.

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Andrew D Morris

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Jayne A L Houghton

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Kevin Colclough

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Maggie Shepherd

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Petra Dusatkova

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Stepanka Pruhova

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Thomas W Laver

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P2860

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

A global reference for human genetic variation

Analysis of protein-coding genetic variation in 60,706 humans

Multidomain integration in the structure of the HNF-4α nuclear receptor complex

Organization and partial sequence of the hepatocyte nuclear factor-4 alpha/MODY1 gene and identification of a missense mutation, R127W, in a Japanese family with MODY

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

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

A role for coding functional variants in HNF4A in type 2 diabetes susceptibility

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

Digenic heterozygous HNF1A and HNF4A mutations in two siblings with childhood-onset diabetes.

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3212-3217

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scholarly article

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10.2337/DB16-0628

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10

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65

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Andrew Tym Hattersley

Kashyap A Patel

Michael N Weedon

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2016-08-02T00:00:00Z

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27486234

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5035684

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