Expanding the Phenotype of Ifap/Breseck Syndrome: A New Case with Severe Hypogammaglobulinemia

AuthID
 P-006-69R
7
Author(s)
Corujeira, S
·
Agueda, S
·
Canelhas, A
·
Rocha, R
·
Tipo de Documento
Article
Year published
2013
Publicado
in EUROPEAN JOURNAL OF MEDICAL GENETICS, ISSN: 1769-7212
Volume: 56, Número: 11, Páginas: 603-605 (3)
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Publication Identifiers
Pubmed: 24090718
SCOPUS: 2-s2.0-84885954035
Wos: WOS:000325993600004
Source Identifiers
ISSN: 1769-7212
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