Functional analysis of a novel POLγA mutation associated with a severe perinatal mitochondrial encephalomyopathy-Reference-Cited by-同舟云学术

Functional analysis of a novel POLγA mutation associated with a severe perinatal mitochondrial encephalomyopathy

Published:2021-04 Issue:4 Volume:31 Page:348-358
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Darin Niklas,Siibak Triinu,Peter Bradley,Hedberg-Oldfors Carola,Kollberg Gittan,Kalbin Vassili,Moslemi Ali-Reza,Macao Bertil,Oldfors Anders,Falkenberg Maria

Funder

Göteborgs Universitet

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Reference37 articles.

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3. Human mitochondrial DNA replication machinery and disease;Young;Curr Opin Genet Dev,2016

4. 155th ENMC workshop: polymerase gamma and disorders of mitochondrial DNA synthesis, 21-23 September 2007, Naarden, The Netherlands;Chinnery;Neuromuscul Disord,2008

5. DNA replication and transcription in mammalian mitochondria;Falkenberg;Annu Rev Biochem,2007

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