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A novel splice site mutation (3157+1G>T) in the dystrophin gene causing total exon skipping and DMD phenotype
Author(s) -
Sironi M.,
Corti S.,
Locatelli F.,
Cagliani R.,
Comi G.P.
Publication year - 2001
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.18
Subject(s) - biology , humanities , philosophy