Child with Unusual Combination of Sickle Cell Disease and Autosomal Recessive Agammaglobulinemia Associated with a Novel Cd79A Gene Mutation

AuthID
P-00Q-8C0
4
Author(s)
Fraga, S
·
Esteves, I
·
Calhau, P
Tipo de Documento
Review
Year published
2019
Publicado
in BMJ Case Reports, ISSN: 1757-790X
Volume: 12, Número: 2
Indexing
Publication Identifiers
SCOPUS: 2-s2.0-85061619081
Source Identifiers
ISSN: 1757-790X
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