Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease.
about
Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease.Overexpression of DNMT3b target genes during Enteric Nervous System development contribute to the onset of Hirschsprung diseaseSporadic Hirschsprung Disease: Mutational Spectrum and Novel Candidate Genes Revealed by Next-generation Sequencing.Hirschsprung disease - integrating basic science and clinical medicine to improve outcomes.Common genetic variants in GAL, GAP43 and NRSN1 and interaction networks confer susceptibility to Hirschsprung disease.
P2860
Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease.
description
2015 nî lūn-bûn
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2015年の論文
@ja
2015年学术文章
@wuu
2015年学术文章
@zh-cn
2015年学术文章
@zh-hans
2015年学术文章
@zh-my
2015年学术文章
@zh-sg
2015年學術文章
@yue
2015年學術文章
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2015年學術文章
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name
Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease.
@ast
Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease.
@en
type
label
Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease.
@ast
Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease.
@en
prefLabel
Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease.
@ast
Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease.
@en
P2093
P2860
P356
P1433
P1476
Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease.
@en
P2093
Ana Torroglosa
Berta Luzón-Toro
Guillermo Antiñolo
Hongsheng Gui
Joaquín Dopazo
Laura Espino-Paisán
Macarena Ruiz-Ferrer
Marta Bleda
María Del Valle Enguix-Riego
María-Mercé García-Barceló
P2860
P2888
P356
10.1038/SREP16473
P407
P577
2015-11-12T00:00:00Z