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3′ acceptor splice site mutation in intron 50 leads to mild duchenne muscular dystrophy phenotype
Author(s) -
Kekou Kiriaki,
Florentin Lina,
Metaxotou Catherine
Publication year - 1998
Publication title -
human mutation
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 162
eISSN - 1098-1004
pISSN - 1059-7794
DOI - 10.1002/humu.1380110168
Subject(s) - pediatrics , unit (ring theory) , university hospital , medicine , family medicine , psychology , mathematics education
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