Biallelic variants in TAMM41 are associated with low muscle cardiolipin levels, leading to neonatal mitochondrial disease-Reference-Cited by-同舟云学术

Biallelic variants in TAMM41 are associated with low muscle cardiolipin levels, leading to neonatal mitochondrial disease

Published:2022-04 Issue:2 Volume:3 Page:100097
ISSN:2666-2477
Container-title:Human Genetics and Genomics Advances
language:en
Short-container-title:Human Genetics and Genomics Advances

Author:

Thompson Kyle,Bianchi Lucas,Rastelli Francesca,Piron-Prunier Florence,Ayciriex Sophie,Besmond Claude,Hubert Laurence,Barth Magalie,Barbosa Inês A.,Deshpande Charu,Chitre Manali,Mehta Sarju G.,Wever Eric J.M.,Marcorelles Pascale,Donkervoort Sandra,Saade Dimah,Bönnemann Carsten G.,Chao Katherine R.,Cai Chunyu,Iannaccone Susan T.,Dean Andrew F.,McFarland Robert,Vaz Frédéric M.,Delahodde Agnès,Taylor Robert W.,Rötig Agnès

Publisher

Elsevier BV

Subject

Genetics (clinical),Molecular Medicine

Reference22 articles.

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3. Tam41 is a CDP-diacylglycerol synthase required for cardiolipin biosynthesis in mitochondria;Tamura;Cell Metab.,2013

4. Remodeling of cardiolipin by phospholipid transacylation;Xu;J. Biol. Chem.,2003

5. A novel X-linked gene, G4.5. is responsible for Barth syndrome;Bione;Nat. Genet.,1996

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