دورية أكاديمية

A −16C>T substitution in the 5′ UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in Nagano

التفاصيل البيبلوغرافية
العنوان: A −16C>T substitution in the 5′ UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in Nagano
المؤلفون: Ohata, TakakoAff1, Aff2, Yoshida, KunihiroAff1, Aff3, Aff4, Sakai, Haruya, Hamanoue, Haruka, Mizuguchi, Takeshi, Shimizu, Yusaku, Okano, Tomomi, Takada, Fumio, Ishikawa, Kinya, Mizusawa, Hidehiro, Yoshiura, Ko-ichiro, Fukushima, Yoshimitsu, Ikeda, Shu-ichi, Matsumoto, Naomichi
المصدر: Journal of Human Genetics. 51(5):461-466
قاعدة البيانات: Springer Nature Journals
الوصف
تدمد:14345161
1435232X
DOI:10.1007/s10038-006-0385-6