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

AuthID
 P-00N-47R
7
Author(s)
Coelho, T
·
Tipo de Documento
Article
Year published
2017
Publicado
in Genes, ISSN: 2073-4425
Volume: 8, Número: 10, Páginas: 253
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Publication Identifiers
SCOPUS: 2-s2.0-85030989811
Source Identifiers
ISSN: 2073-4425
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