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The Δ327 mutation in the fanconi anemia group C gene generates a novel transcript lacking the first two coding exons
Author(s) -
Parker Linda,
Santos Claudia Dos,
Buchwald Manuel
Publication year - 1998
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/humu.1380110187
Subject(s) - medical genetics , sick child , library science , genetics , medicine , family medicine , biology , pediatrics , gene , computer science
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