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A novel missense mutation (H119L) identified in a Taiwan Chinese family with glycogen storage disease Ia (Von Gierke disease)
Author(s) -
Wu MeiChen,
Tsai Fuujen,
Lee ChengChun,
Tsai ChangHai,
Wu JerYuarn
Publication year - 2000
Publication title -
human mutation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 162
eISSN - 1098-1004
pISSN - 1059-7794
DOI - 10.1002/1098-1004(200011)16:5<447::aid-humu17>3.0.co;2-m
Subject(s) - china , medicine , family medicine , university hospital , pediatrics , history , archaeology