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Autosomal dominant cerebellar ataxia type I in Morocco: presence of the SCA1 and SCA3/MJD mutations

✍ Scribed by A. Benomar; F. Meggouh; O. Didierjean; N. Kissani; A. Dürr; A. Sefiani; T. Chkili; Y. Agid; M. Yahyaoui; A. Brice

Book ID: 115236143
Publisher: John Wiley and Sons
Year: 1996
Tongue: English
Weight: 256 KB
Volume: 3
Category: Article
ISSN: 1351-5101
DOI: 10.1111/j.1468-1331.1996.tb00231.x

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