Homozygous missense mutation in UQCRC2 associated with severe encephalomyopathy, mitochondrial complex III assembly defect and activation of mitochondrial protein quality control-Reference-Cited by-同舟云学术

Homozygous missense mutation in UQCRC2 associated with severe encephalomyopathy, mitochondrial complex III assembly defect and activation of mitochondrial protein quality control

Published:2021-08 Issue:8 Volume:1867 Page:166147
ISSN:0925-4439
Container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Author:

Burska Daniela,Stiburek Lukas,Krizova Jana,Vanisova Marie,Martinek Vaclav,Sladkova Jana,Zamecnik Josef,Honzik Tomas,Zeman Jiri,Hansikova Hana,Tesarova Marketa

Funder

Ministerstvo zdravotnictví České republiky

Univerzita Karlova

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

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