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
Document Type
Review
Year published
2019
Published
in BMJ Case Reports, ISSN: 1757-790X
Volume: 12, Issue: 2
Indexing
Scopus®
Google Scholar®
Publication Identifiers
Scopus: 2-s2.0-85061619081
Source Identifiers
ISSN: 1757-790X
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