Hereditary Spherocytosis with Total Absence of Band 3 in a Baby with Mutation Coimbra (V488M) in the Homozygous State.

AuthID
 P-001-AAB
11
Author(s)
Alloisio, N
·
Almeida, H
·
Texier, P
·
Lemos, C
·
Mimoso, C
·
Morle, L
·
BeyCabet, F
·
Rudigoz, RC
·
Delaunay, J
·
Tamagnini, G
Document Type
Abstract
Year published
1997
Published
in BLOOD, ISSN: 0006-4971
Volume: 90, Issue: 10, Pages: 1164-1164 (1)
Indexing
Wos®
Publication Identifiers
Wos: WOS:A1997YG42401163
Source Identifiers
ISSN: 0006-4971
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