| Literature DB >> 9416823 |
A Destee1, F Cassim, L Defebvre, J D Guieu.
Abstract
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 essential myoclonus.Entities:
Mesh：
Year: 1997 PMID： 9416823 PMCID： PMC2169870 DOI： 10.1136/jnnp.63.6.804
Source DB: PubMed Journal: J Neurol Neurosurg Psychiatry ISSN： 0022-3050 Impact factor: 10.154