Molecular Study of Congenital Erythrocytosis in 70 Unrelated Patients Revealed a Potential Causal Mutation in Less than Half of the Cases (Where Is/Are the Missing Gene(S)?)

AuthID
 P-006-6TN
18
Author(s)
Almeida, H
·
Relvas, L
·
Oliveira, AC
·
Rossi, C
·
Fernandez Lago, C
·
Araujo, AL
·
Silva, J
·
Vitoria, H
·
Miguel, N
·
Martin Nunez, G
·
Document Type
Article
Year published
2013
Published
in EUROPEAN JOURNAL OF HAEMATOLOGY, ISSN: 0902-4441
Volume: 91, Issue: 4, Pages: 361-368 (8)
Indexing
Wos®
Scopus®
Crossref®3
Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 23859443
SCOPUS: 2-s2.0-84884815245
Wos: WOS:000325035000010
Source Identifiers
ISSN: 0902-4441
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