FASTKD2 nonsense mutation in an infantile mitochondrial encephalomyopathy associated with cytochrome c oxidase deficiency

GHEZZI D

•

SAADA A

•

D'ADAMO, ADAMO PIO

altro

ZEVIANI M.

2008

journal article

Periodico

AMERICAN JOURNAL OF HUMAN GENETICS

DOI

10.1016/j.ajhg.2008.08.009

WOS

WOS:000259307200012

Archivio

http://hdl.handle.net/11368/1854200

info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-50949096038

Diritti

metadata only access

Web of Science© citazioni

83

Data di acquisizione
Mar 23, 2024