スポンサーリンク
Department of Medical Genetics, Kitasato University Graduate School of Medical Sciences | 論文
- Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemia
- A -16C>T substitution in the 5' UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in Nagano