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Different attenuated phenotypes of GM2 gangliosidosis variant B in Japanese patients withHEXAmutations at codon 499, and five novel mutations responsible for infantile acute form

✍ Scribed by Akemi Tanaka; LanThiNgcok Hoang; Yasuaki Nishi; Satoshi Maniwa; Makio Oka; Tsunekazu Yamano


Publisher
Nature Publishing Group
Year
2003
Tongue
English
Weight
174 KB
Volume
48
Category
Article
ISSN
1435-232X

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