Identification of a novel termination codon mutation (TAA-->TAT, Term-- >Tyr) in the alpha 2 globin gene of a Laotian girl with hemoglobin H disease [letter]
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Overview
status
publication date
- June 1, 1994
has subject area
- 1102 Cardiorespiratory Medicine and Haematology (FoR)
- 1103 Clinical Sciences (FoR)
- 1114 Paediatrics and Reproductive Medicine (FoR)
- Base Sequence (MeSH)
- Child (MeSH)
- Codon (MeSH)
- Female (MeSH)
- Globins (MeSH)
- Humans (MeSH)
- Immunology (Science Metrix)
- Molecular Sequence Data (MeSH)
- Mutation (MeSH)
- alpha-Thalassemia (MeSH)
published in
- Blood Journal