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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Atrophy and SCA19[original query]
Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families.
Archives of neurology 2004 May 61 (5): 727-33.
Brusco Alfredo, Gellera Cinzia, Cagnoli Claudia, Saluto Alessandro, Castucci Alessia, Michielotto Chiara, Fetoni Vincenza, Mariotti Caterina, Migone Nicola, Di Donato Stefano, Taroni Fran
Analysis of SCA8, SCA10, SCA12, SCA17 and SCA19 in patients with unknown spinocerebellar ataxia: a Thai multicentre study.
BMC neurology 2015 15 (1): 166.
Choubtum Lulin, Witoonpanich Pirada, Hanchaiphiboolkul Suchat, Bhidayasiri Roongroj, Jitkritsadakul Onanong, Pongpakdee Sunsanee, Wetchaphanphesat Suppachok, Boonkongchuen Pairoj, Pulkes Teerato
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