J. Vaughan et al., THE ALPHA-SYNUCLEIN ALA53THR MUTATION IS NOT A COMMON-CAUSE OF FAMILIAL PARKINSONS-DISEASE - A STUDY OF 230 EUROPEAN CASES, Annals of neurology, 44(2), 1998, pp. 270-273
We report the results of a screen of 230 European familiar index cases
of Parkinson's disease for the recently described Ala53Thr mutation i
n the alpha-synuclein gene in an autosomal dominant Parkinson's diseas
e kindred. No mutations were found from this broad white population, a
nd we therefore conclude that although of great interest, this mutatio
n is a very rare cause of familial Parkinson's disease.