NRG1 variant effects in patients with Hirschsprung disease

about

NRG1 variant effects in patients with Hirschsprung disease

Item

http://www.wikidata.org/entity/Q58765280

description

im September 2018 veröffentlichter wissenschaftlicher Artikel

@de

scientific article published on 04 September 2018

@en

wetenschappelijk artikel

@nl

наукова стаття, опублікована у вересні 2018

@uk

name

NRG1 variant effects in patients with Hirschsprung disease

@en

NRG1 variant effects in patients with Hirschsprung disease

@nl

type

Item

label

NRG1 variant effects in patients with Hirschsprung disease

@en

NRG1 variant effects in patients with Hirschsprung disease

@nl

prefLabel

NRG1 variant effects in patients with Hirschsprung disease

@en

NRG1 variant effects in patients with Hirschsprung disease

@nl

P1476

NRG1 variant effects in patients with Hirschsprung disease

@en

P2093

Akhmad Makhmudi

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

Alvin Santoso Kalim

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

Indra Adrianto

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

Lai Poh San

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

Nova Yuli Prasetyo Budi

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

Raman Sethi

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

Taufik Indrawan

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

P2860

Identification of heregulin, a specific activator of p185erbB2

Contribution of rare and common variants determine complex diseases-Hirschsprung disease as a model

Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease

Natural Selection and Functional Potentials of Human Noncoding Elements Revealed by Analysis of Next Generation Sequencing Data

Two novel mutations in the ED1 gene in Japanese families with X-linked hypohidrotic ectodermal dysplasia.

The utility of the hematoxylin and eosin staining in patients with suspected Hirschsprung disease.

Differential contributions of rare and common, coding and noncoding Ret mutations to multifactorial Hirschsprung disease liability

Three major lineages of Asian Y chromosomes: implications for the peopling of east and southeast Asia.

Comprehensive analysis of NRG1 common and rare variants in Hirschsprung patients

Hirschsprung disease, associated syndromes and genetics: a review.

P2888

s12887-018-1265-x

P304

292

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

P31

scholarly article

P356

10.1186/S12887-018-1265-X

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

P407

English

P433

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

P478

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

P50

Kristy Iskandar

Aditya Rifqi Fauzi

Gunadi

P577

2018-09-04T00:00:00Z

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

P6179

1106660892

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

P698

30180823

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

P932

6123906

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