Phenotypic Variability in a Portuguese Family With X-Linked Creatine Transport Deficiency

AuthID
 P-002-HAE
5
Author(s)
Rodrigues, F
·
Valongo, C
·
Salomons, GS
·
Tipo de Documento
Article
Year published
2012
Publicado
in PEDIATRIC NEUROLOGY, ISSN: 0887-8994
Volume: 46, Número: 1, Páginas: 39-41 (3)
Indexing
Wos®
Scopus®
Crossref®5
Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 22196490
SCOPUS: 2-s2.0-84555202539
Wos: WOS:000299065000006
Source Identifiers
ISSN: 0887-8994
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