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HOMOZYGOUS NON‐DELETION α 2 GLOBIN GENE MUTATION (INITIATION CODON MUTATION): CLINICAL AND HAEMATOLOGICAL PHENOTYPE
Author(s) -
Galanello R.,
Monne M. I.,
Paderi L.,
Paglietti E.,
Atzori G.,
Addis M.,
Limongelli O.,
Cao A.,
Macciotta A.
Publication year - 1991
Publication title -
british journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.907
H-Index - 186
eISSN - 1365-2141
pISSN - 0007-1048
DOI - 10.1111/j.1365-2141.1991.tb08018.x
Subject(s) - mutation , phenotype , genetics , gene , biology , globin , microbiology and biotechnology