Mutations in TTC19: expanding the molecular, clinical and biochemical phenotype.
about
Leigh syndrome: One disorder, more than 75 monogenic causes.LYRM7 mutations cause a multifocal cavitating leukoencephalopathy with distinct MRI appearance.Oxidative Phosphorylation System in Gastric Carcinomas and Gastritis.Combined Respiratory Chain Deficiency and UQCC2 Mutations in Neonatal Encephalomyopathy: Defective Supercomplex Assembly in Complex III DeficienciesHuman diseases associated with defects in assembly of OXPHOS complexes
P2860
Mutations in TTC19: expanding the molecular, clinical and biochemical phenotype.
description
2015 nî lūn-bûn
@nan
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
2015年论文
@zh
2015年论文
@zh-cn
name
Mutations in TTC19: expanding the molecular, clinical and biochemical phenotype.
@ast
Mutations in TTC19: expanding the molecular, clinical and biochemical phenotype.
@en
type
label
Mutations in TTC19: expanding the molecular, clinical and biochemical phenotype.
@ast
Mutations in TTC19: expanding the molecular, clinical and biochemical phenotype.
@en
prefLabel
Mutations in TTC19: expanding the molecular, clinical and biochemical phenotype.
@ast
Mutations in TTC19: expanding the molecular, clinical and biochemical phenotype.
@en
P2093
P2860
P1476
Mutations in TTC19: expanding the molecular, clinical and biochemical phenotype.
@en
P2093
Christian Rauscher
Esther M Maier
Franz A Zimmermann
Hans P Wagentristl
Johannes Koch
Peter Freisinger
Rainer Seidl
René G Feichtinger
Tobias B Haack
Uwe Ahting
P2860
P2888
P356
10.1186/S13023-015-0254-5
P577
2015-04-02T00:00:00Z
P5875
P6179
1038129702