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Distal hereditary upper limb muscular atrophy

OBJECTIVES—To identify the clinical, electrophysiological, and genetic characteristics of a family with an unusual form of hereditary motor neuron disease.
METHODS—Surviving members of a pedigree in which affected members presented with weakness and atrophy of distal musculature in the upper limbs w...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Gross, D, Rajput, A, Yeung, M
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: BMJ Group 1998
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC2169965/
https://ncbi.nlm.nih.gov/pubmed/9489534
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