Aldolase A deficiency: Report of new cases and literature review
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology
Reference13 articles.
1. Molecular gene mapping of human aldolase A (ALDOA) gene to chromosome 16;Kukita;Hum. Genet.,1987
2. Red cell aldolase deficiency and hemolytic anemia: a new syndrome;Beutler;Trans. Assoc. Am. Phys.,1973
3. Two cases of red cell aldolase deficiency associated with hereditary hemolytic anemia in a Japanese family;Miwa;Am. J. Hematol.,1981
4. Human aldolase a deficiency associated with a hemolytic anemia: thermolabile aldolase due to a single base mutation;Kishi;Proc Natl AcadSci U S A.,1987
5. Brief report: inherited metabolic myopathy and hemolysis due to a mutation in aldolase A;Kreuder;N. Engl. J. Med.,1996
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