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A case of late-onset Segawa syndrome (autosomal dominant dopa-responsive dystonia) with a novel mutation of the GTP-cyclohydrase I (GCH1) gene

โœ Scribed by Hirokazu Furuya; Hiroyuki Murai; Kazuo Takasugi; Yasumasa Ohyagi; Fumi Urano; Taroh Kishi; Hiroshi Ichinose; Jun-ichi Kira


Book ID
116369008
Publisher
Elsevier Science
Year
2006
Tongue
English
Weight
226 KB
Volume
108
Category
Article
ISSN
0303-8467

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