Ocular mitochondrial myopathy evolving late in life into a disabling proximal myopathy associated with the mitochondrial DNA 3243 A to G mutation.


Autoria(s): Hirt L.; Maréchal C.; Ghika J.A.; Magistretti P.J.; Bogousslavsky J.
Data(s)

2001

Identificador

http://serval.unil.ch/?id=serval:BIB_F071C2247830

isbn:0340-5354

pmid:11374101

doi:10.1007/s004150170211

isiid:000168385400014

Idioma(s)

en

Fonte

Journal of neurology, vol. 248, no. 4, pp. 332-3

Palavras-Chave #Aged; Aged, 80 and over; DNA, Mitochondrial; Disabled Persons; Disease Progression; Humans; Male; Mitochondrial Myopathies; Point Mutation; Polymerase Chain Reaction
Tipo

info:eu-repo/semantics/article

article