Associated Papers
Molecular expression, characterization and mechanism of ALAS2 gain-of-function mutants.
Tchaikovskii V et al.
Molecular Medicine (cambridge, Mass.), 2019
30678654 (PubMed )
Supplement: 10020_2019_70_MOESM2_ESM.doc
Hereditary sideroblastic anaemia due to a mutation in exon 10 of the erythroid 5-aminolaevulinate synthase gene.
Edgar AJ et al.
British Journal of Haematology, 1998
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