Possible X linked congenital mitochondrial cardiomyopathy in three families
about
Barth's syndrome-like disorder: a new phenotype with a maternally inherited A3243G substitution of mitochondrial DNA (MELAS mutation).X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome.X chromosome inactivation in carriers of Barth syndrome.The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies.Clinicopathologic conference: Barth Syndrome.
P2860
Possible X linked congenital mitochondrial cardiomyopathy in three families
description
1993 nî lūn-bûn
@nan
1993 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
name
Possible X linked congenital mitochondrial cardiomyopathy in three families
@ast
Possible X linked congenital mitochondrial cardiomyopathy in three families
@en
type
label
Possible X linked congenital mitochondrial cardiomyopathy in three families
@ast
Possible X linked congenital mitochondrial cardiomyopathy in three families
@en
prefLabel
Possible X linked congenital mitochondrial cardiomyopathy in three families
@ast
Possible X linked congenital mitochondrial cardiomyopathy in three families
@en
P2093
P2860
P356
P1476
Possible X linked congenital mitochondrial cardiomyopathy in three families
@en
P2093
Hellebostad M
Langslet A
Orstavik KH
Skjörten F
P2860
P304
P356
10.1136/JMG.30.4.269
P407
P577
1993-04-01T00:00:00Z