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
·
Document Type
Article
Year published
2008
Published
in MOLECULAR GENETICS AND METABOLISM, ISSN: 1096-7192
Volume: 93, Issue: 1, Pages: 66-73 (8)
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Scopus®
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Pubmed®
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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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