75 Prevalence of mitochondrial gene defects in maternally inherited diabetes and deafness and in neuromuscular presentations suggesting respiratory chain dysfunction: Screening of the entire mitochondrial genome in 100 patients

Autor:	Véronique Paquis-Flucklinger, Claude Desnuelle, C. Rouzier, Jean Pouget, Jean-François Pellissier, D. Raccah, Tahseen Mozaffar, J. Abdenur, Sylvie Bannwarth, J. Jay Gargus, Mariella Simon, Douglas C. Wallace, Vincent Procaccio, Brigitte Chabrol, J.C. Lambert, Jason C. Poole, B. Vialettes
Rok vydání:	2007
Předmět:	Genetics Mitochondrial DNA Diabetes mellitus medicine Molecular Medicine Cell Biology Respiratory chain dysfunction Biology medicine.disease Molecular Biology
Zdroj:	Mitochondrion. 7:426
ISSN:	1567-7249
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::55b5527c4a06a912c0ce25b9901b3db5 https://doi.org/10.1016/j.mito.2007.08.079 Zobrazit plný text záznamu Full Text from ScienceDirect