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Oculopharyngeal involvement in familial neurogenic muscular atrophy

A Japanese family with progressive spinal muscular atrophy is presented. Seven members in two generations were affected and the mode of inheritance was probably an autosomal recessive trait. A characteristic feature of this family was the presence of oculopharyngeal involvement in some of the affect...

Cur síos iomlán

Sábháilte in:
Sonraí bibleagrafaíochta
Foilsithe in:J Neurol Neurosurg Psychiatry
Príomhchruthaitheoirí: Matsunaga, M., Inokuchi, T., Ohnishi, A., Kuroiwa, Y.
Formáid: Artigo
Teanga:Inglês
Foilsithe / Cruthaithe: BMJ Publishing Group 1973
Ábhair:
Rochtain ar líne:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC494283/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/4691681/
https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jnnp.36.1.104
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