Atypical Hemolytic-Uremic Syndrome: Recurrent Phenotypic Expression of a Patient with Mcp Gene Mutation Combined with Risk Haplotypes

AuthID
 P-00Q-798
7
Author(s)
Marini, SC
·
Guilherme, R
·
Carda, JP
·
Pinto, CS
·
Fidalgo, T
·
Tipo de Documento
Article
Year published
2019
Publicado
in BLOOD COAGULATION & FIBRINOLYSIS, ISSN: 0957-5235
Volume: 30, Número: 2, Páginas: 68-70 (3)
Indexing
Wos®
Scopus®
Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 30676336
SCOPUS: 2-s2.0-85061295647
Wos: WOS:000472685000004
Source Identifiers
ISSN: 0957-5235
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