Double mutation (A171T and D444H) is a common cause of profound biotinidase deficiency in children ascertained by newborn screening the the United States. Mutations in brief no. 128. Online.
暂无分享,去创建一个
G. Buck | B. Wolf | K. L. Swango | J. Hymes | K. Norrgard | R. Pomponio | T. Reynolds | Barry Wolf | Gregory A. Buck