Early onset severe myopathy due to the A3302G mutation in the mitochondrial tRNA LEU(UUR).


Autoria(s): Hahn D.; Schaller A.; Gallati S.; Ballhausen D.; Jacquemont S.; Jeannet P.Y.; Bonafé L.; Nuoffer J.M.
Data(s)

2007

Identificador

http://serval.unil.ch/?id=serval:BIB_FA71A3AF0784

isbn:1573-2665

isiid:000248860000286

Idioma(s)

en

Fonte

44th Annual Symposium of the Society for the Study of Inborn Errors of Metabolism

Tipo

info:eu-repo/semantics/conferenceObject

inproceedings