Novel Synonymous Substitution in Pomgnt1 Promotes Exon Skipping in a Patient with Congenital Muscular Dystrophy

AuthID
 P-003-Z0X
11
Author(s)
Fokkema, I
·
Goncalves, A
·
Cabral, A
·
Diogo, L
·
Galan, L
·
Guimaraes, A
·
Fineza, I
·
den Dunnen, JT
·
Tipo de Documento
Article
Year published
2008
Publicado
in JOURNAL OF HUMAN GENETICS, ISSN: 1434-5161
Volume: 53, Número: 6, Páginas: 565-572 (8)
Indexing
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Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 18330676
SCOPUS: 2-s2.0-44449085738
Wos: WOS:000256320100012
Source Identifiers
ISSN: 1434-5161
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