Occipital Horn Syndrome and Classical Menkes Syndrome Caused by Deep Intronic Mutations, Leading to the Activation of Atp7A Pseudo-Exon

AuthID
 P-009-7Q9
9
Author(s)
Yasmeen, S
·
Lund, K
·
De Paepe, A
·
Heiberg, A
·
Silva, J
·
Martins, M
·
Moller, LB
Document Type
Article
Year published
2014
Published
in EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN: 1018-4813
Volume: 22, Issue: 4, Pages: 517-521 (5)
Indexing
Wos®
Scopus®
Crossref®
Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 24002164
Scopus: 2-s2.0-84896546344
Wos: WOS:000332938400022
Source Identifiers
ISSN: 1018-4813
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