Defining functional classes of Barth syndrome mutation in humans-Reference-Cited by-同舟云学术

Defining functional classes of Barth syndrome mutation in humans

Published:2016-02-16 Issue:9 Volume:25 Page:1754-1770
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum. Mol. Genet.

Author:

Lu Ya-Wen,Galbraith Laura,Herndon Jenny D.,Lu Ya-Lin,Pras-Raves Mia,Vervaart Martin,Van Kampen Antoine,Luyf Angela,Koehler Carla M.,McCaffery J.Michael,Gottlieb Eyal,Vaz Frederic M.,Claypool Steven M.

Funder

Barth Syndrome Foundation

National Institutes of Health

NIH/ORIP

American Heart Association

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/25/9/1754/18527991/ddw046.pdf

Reference55 articles.

1. The complexity of cardiolipin in health and disease

2. Mitochondrial Phosphatase PTPMT1 Is Essential for Cardiolipin Biosynthesis

3. Cardiolipin, a critical determinant of mitochondrial carrier protein assembly and function

4. Mitochondrial Cardiolipin Involved in Outer-Membrane Protein Biogenesis: Implications for Barth Syndrome

5. The translocator maintenance protein Tam41 is required for mitochondrial cardiolipin biosynthesis

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