Exonization of an Intronic Line-1 Element Causing Becker Muscular Dystrophy as a Novel Mutational Mechanism in Dystrophin Gene

AuthID
 P-00N-805
7
Author(s)
Sousa, M
·
Tipo de Documento
Article
Year published
2017
Publicado
in GENES, ISSN: 2073-4425
Volume: 8, Número: 10
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Publication Identifiers
Wos: WOS:000414862300018
Source Identifiers
ISSN: 2073-4425
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