Cln2/Tpp1 Deficiency: The Novel Mutation Ivs7-10A>G Causes Intron Retention and Is Associated with a Mild Disease Phenotype

AuthID
 P-004-467
9
Author(s)
Dias, A
·
Loureiro, L
·
Guimaraes, A
·
Tipo de Documento
Article
Year published
2008
Publicado
in MOLECULAR GENETICS AND METABOLISM, ISSN: 1096-7192
Volume: 93, Número: 1, Páginas: 66-73 (8)
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Publication Identifiers
Pubmed: 17959406
SCOPUS: 2-s2.0-36849026004
Wos: WOS:000252581300011
Source Identifiers
ISSN: 1096-7192
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