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NovelSPG6 mutation p.A100T in a Japanese family with autosomal dominant form of hereditary spastic paraplegia

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author: Peter Henry St George-Hyslop  Toshitaka Kawarai  Giorgio Bernardi  Shabnam Salehi-Rad  Ekaterina Rogaeva  Christine Sato  Antonio Orlacchio 

Publication date 2006
Language English
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