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Volumn 89, Issue 10, 1997, Pages 3888-
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A novel/β+-thalassemia mutation (codon 10 GCC → GCA) and a rare transcriptional mutation (28a →G) in Indians [1]
a a a
a
KEM HOSPITAL
(India)
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Author keywords
[No Author keywords available]
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Indexed keywords
BETA GLOBIN;
BETA THALASSEMIA;
CASE REPORT;
CHILD;
FAMILY STUDY;
FEMALE;
GENE MUTATION;
GLOBIN GENE;
HUMAN;
INDIA;
LETTER;
MALE;
NUCLEIC ACID BASE SUBSTITUTION;
PEDIGREE;
PRESCHOOL CHILD;
PRIORITY JOURNAL;
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EID: 0031009450
PISSN: 00064971
EISSN: None
Source Type: Journal
DOI: 10.1182/blood.v89.10.3888 Document Type: Letter |
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Times cited : (11)
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References (8)
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