Variants in the MIPEP gene presenting with complex neurological phenotype without cardiomyopathy, impair OXPHOS protein maturation and lead to a reduced OXPHOS abundance in patient cells-Reference-Cited by-同舟云学术

Variants in the MIPEP gene presenting with complex neurological phenotype without cardiomyopathy, impair OXPHOS protein maturation and lead to a reduced OXPHOS abundance in patient cells

Published:2021-11 Issue:3 Volume:134 Page:267-273
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Pulman Juliette,Ruzzenente Benedetta,Horak Martin,Barcia Giulia,Boddaert Nathalie,Munnich Arnold,Rötig Agnès,Metodiev Metodi D.

Funder

French Muscular Dystrophy Association

Agence Nationale de la Recherche

AFM-Téléthon

Fondation Bettencourt Schueller

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference28 articles.

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3. MIP1, a new yeast gene homologous to the rat mitochondrial intermediate peptidase gene, is required for oxidative metabolism in Saccharomyces cerevisiae;Isaya;Mol. Cell. Biol.,1994

4. Amino-terminal octapeptides function as recognition signals for the mitochondrial intermediate peptidase;Isaya;J. Biol. Chem.,1992

5. Rat liver mitochondrial intermediate peptidase (MIP): purification and initial characterization;Kalousek;EMBO J.,1992

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