Identification of candidate genes for histiocytoid cardiomyopathy (HC) using whole genome expression analysis: analyzing material from the HC registry.
about
Histiocytoid cardiomyopathy and microphthalmia with linear skin defects syndrome: phenotypes linked by truncating variants in NDUFB11.Association of ventricular noncompaction and histiocytoid cardiomyopathy: case report and review of the literature.Exome sequencing of patients with histiocytoid cardiomyopathy reveals a de novo NDUFB11 mutation that plays a role in the pathogenesis of histiocytoid cardiomyopathy
P2860
Identification of candidate genes for histiocytoid cardiomyopathy (HC) using whole genome expression analysis: analyzing material from the HC registry.
description
2011 nî lūn-bûn
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2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Identification of candidate ge ...... material from the HC registry.
@ast
Identification of candidate ge ...... material from the HC registry.
@en
type
label
Identification of candidate ge ...... material from the HC registry.
@ast
Identification of candidate ge ...... material from the HC registry.
@en
prefLabel
Identification of candidate ge ...... material from the HC registry.
@ast
Identification of candidate ge ...... material from the HC registry.
@en
P2093
P2860
P356
P1476
Identification of candidate ge ...... material from the HC registry.
@en
P2093
Bahig M Shehata
Carlos S Moreno
Charlotte K Steelman
Gigi K Davis
Mark Bouzyk
Sarah C Shulman
Weining Tang
P2860
P304
P356
10.2350/10-05-0826-OA.1
P577
2011-05-17T00:00:00Z