Identification of Rare Variants in ATP8B4 as a Risk Factor for Systemic Sclerosis by Whole-Exome Sequencing.
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Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing studyUnfolding the pathogenesis of scleroderma through genomics and epigenomics.Working your SOCS off: The role of ASB10 and protein degradation pathways in glaucoma.Systematic approach to understanding the pathogenesis of systemic sclerosis.Brief Report: Whole-Exome Sequencing for Identification of Potential Causal Variants for Diffuse Cutaneous Systemic Sclerosis.Ubiquitination in Scleroderma Fibrosis and Its Treatment
P2860
Identification of Rare Variants in ATP8B4 as a Risk Factor for Systemic Sclerosis by Whole-Exome Sequencing.
description
2015 nî lūn-bûn
@nan
2015 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
name
Identification of Rare Variant ...... osis by Whole-Exome Sequencing
@nl
Identification of Rare Variant ...... sis by Whole-Exome Sequencing.
@ast
Identification of Rare Variant ...... sis by Whole-Exome Sequencing.
@en
type
label
Identification of Rare Variant ...... osis by Whole-Exome Sequencing
@nl
Identification of Rare Variant ...... sis by Whole-Exome Sequencing.
@ast
Identification of Rare Variant ...... sis by Whole-Exome Sequencing.
@en
prefLabel
Identification of Rare Variant ...... osis by Whole-Exome Sequencing
@nl
Identification of Rare Variant ...... sis by Whole-Exome Sequencing.
@ast
Identification of Rare Variant ...... sis by Whole-Exome Sequencing.
@en
P2093
P2860
P3181
P356
P1476
Identification of Rare Variant ...... sis by Whole-Exome Sequencing.
@en
P2093
Alan E Berger
Candelaria Vergara
Chris Cheadle
Deborah A Nickerson
Ingo Ruczinski
Kathleen C Barnes
Laura K Hummers
Margaret A Taub
Mary J Emond
P2860
P304
P3181
P356
10.1002/ART.39449
P407
P577
2015-10-16T00:00:00Z