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T313M PINK1 mutation in an extended highly consanguineous saudi family with early-onset parkinson disease
Journal article   Open access

T313M PINK1 mutation in an extended highly consanguineous saudi family with early-onset parkinson disease

Muhammad A Chishti, Saeed Bohlega, Maqbool Ahmed, Arslan Loualich, Pamela Carroll, Christine Sato, Peter ST GEORGE-HYSLOP, David Westaway and Ekaterina Rogaeva
Archives of neurology (Chicago), Vol.63(10), pp.1483-1485
01/10/2006
PMID: 17030667

Abstract

Biological and medical sciences Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy Medical sciences Nervous system (semeiology, syndromes) Neurology
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https://doi.org/10.1001/archneur.63.10.1483View
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