Different attenuated phenotypes of GM2 gangliosidosis variant B in Japanese patients withHEXAmutations at codon 499, and five novel mutations responsible for infantile acute form
Akemi Tanaka, LanThiNgcok Hoang, Yasuaki Nishi, Satoshi Maniwa, Makio Oka, Tsunekazu YamanoVolume:
48
Language:
english
Pages:
4
DOI:
10.1007/s10038-003-0080-9
Date:
November, 2003
File:
PDF, 174 KB
english, 2003