Segregation study in family with severe variant of the A3302G mutation in the mitochondrial tRNA LEU (UUR)


Autoria(s): Ballhausen D.; Guerry F.; Hahn D.; Bonafe L.; Jacquemont S.
Data(s)

2008

Identificador

http://serval.unil.ch/?id=serval:BIB_94A558B3E354

isbn:0141-8955

isiid:000258656400218

doi:10.1007/s10545-008-9975-0

Idioma(s)

en

Fonte

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

Tipo

info:eu-repo/semantics/conferenceObject

inproceedings