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Hereditary chin trembling or hereditary chin myoclonus?

Hereditary chin trembling is a rare autosomal dominant disease often considered as an "essential tremor variant". The clinical and neurophysiological data obtained in a new white family lead to the suggestion that this abnormal involuntary movement is a focal variant of hereditary essentia...

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Detalles Bibliográficos
Main Authors: Destee, A, Cassim, F, Defebvre, L, Guieu, J
Formato: Artigo
Idioma:Inglês
Publicado: BMJ Group 1997
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC2169870/
https://ncbi.nlm.nih.gov/pubmed/9416823
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