T313M PINK1 mutation in an extended highly consanguineous Saudi family with early-onset Parkinson disease.
Chishti MA; Bohlega S; Ahmed M; Loualich A; Carroll P; Sato C; St George-Hyslop P; Westaway D; Rogaeva E; Archives Of Neurology, 2006, vol. 63, issue 10, p 1483, ISSN 00039942. ISBN 00039942.

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