Deficiency of tetralinoleoyl-cardiolipin in Barth syndrome (Q40719070)

23 September 2017

title

Deficiency of tetralinoleoyl-cardiolipin in Barth syndrome (English)

1 reference

23 September 2017

5

Salvatore DiMauro

1 reference

23 September 2017

2

Jeffrey A Towbin

1 reference

23 September 2017

1

Michael Schlame

1 reference

23 September 2017

Paul M Heerdt

3

1 reference

23 September 2017

Roswitha Jehle

series ordinal

4

1 reference

23 September 2017

Thomas J J Blanck

series ordinal

6

1 reference

23 September 2017

publication date

1 May 2002

1 reference

23 September 2017

1 reference

23 September 2017

volume

51

1 reference

23 September 2017

issue

5

1 reference

23 September 2017

page(s)

634-637

1 reference

X-linked cardioskeletal myopathy and neutropenia (Barth syndrome) (MIM 302060)

23 September 2017

cites work

1 reference

X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduria

21 January 2018

1 reference

A novel X-linked gene, G4.5. is responsible for Barth syndrome

21 January 2018

1 reference

The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies.

21 January 2018

1 reference

An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes

21 January 2018

1 reference

Barth syndrome may be due to an acyltransferase deficiency

21 January 2018

1 reference

Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndrome

21 January 2018

1 reference

The biosynthesis and functional role of cardiolipin

21 January 2018

1 reference

Lysocardiolipin formation and reacylation in isolated rat liver mitochondria

21 January 2018

1 reference

Barth's syndrome-like disorder: a new phenotype with a maternally inherited A3243G substitution of mitochondrial DNA (MELAS mutation).

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/ANA.10176

1 reference

23 September 2017

1 reference