The natural history of SCO2 deficiency in 36 Polish children confirmed the genotype–phenotype correlation-Reference-Cited by-同舟云学术

The natural history of SCO2 deficiency in 36 Polish children confirmed the genotype–phenotype correlation

Published:2013-11 Issue:6 Volume:13 Page:810-816
ISSN:1567-7249
Container-title:Mitochondrion
language:en
Short-container-title:Mitochondrion

Author:

Pronicka Ewa,Piekutowska-Abramczuk Dorota,Szymańska-Dębińska Tamara,Bielecka Liliana,Kowalski Paweł,Łuczak Sylwia,Karkucińska-Więckowska Agnieszka,Migdał Marek,Kubalska Jolanta,Zimowski Janusz,Jamroz Ewa,Wierzba Jolanta,Sykut-Cegielska Jolanta,Pronicki Maciej,Zaremba Jacek,Krajewska-Walasek Małgorzata

Funder

Ministry of Science and Higher Education

National Science Centre

CMHI

EU Structural Funds

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Molecular Medicine

Reference35 articles.

1. Retrospective, multicentric study of 180 children with cytochrome c oxidase deficiency;Bohm;Pediatr. Res.,2006

2. Sequence analysis of the structural nuclear encoded subunits and assembly genes of cytochrome c oxidase in a cohort of 10 isolated complex IV-deficient patients revealed five mutations;Coenen;J. Child Neurol.,2006