Sideroblastic anaemias

[1] Mutation of a putative mitochondrial iron transporter gene (ABC7) in X-linked sideroblastic anemia and ataxia (XLSA/A) [J]. HUMAN MOLECULAR GENETICS, 1999, 8 (05) : 743 - 749

[2] AUTOSOMAL INHERITANCE OF SIDEROBLASTIC ANEMIA [J]. CLINICAL AND LABORATORY HAEMATOLOGY, 1988, 10 (03): : 347 - 353

[3] GAMMA-AMINOLEVULINIC ACID SYNTHETASE IN ERYTHROBLASTS OF PATIENTS WITH PYRIDOXINE-RESPONSIVE ANEMIA - HYPERCATABOLISM CAUSED BY THE INCREASED SUSCEPTIBILITY TO THE CONTROLLING PROTEASE [J]. JOURNAL OF CLINICAL INVESTIGATION, 1979, 64 (05) : 1196 - 1203

[4] ASHKENAZI A, 1973, PEDIATRICS, V52, P525

[5] Balduini CL, 1999, HAEMATOLOGICA, V84, P12

[6] A nuclear defect in the 4p16 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndrome [J]. JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (07) : 1570 - 1576

[7] Involvement of mitochondrial ferredoxin and Cox15p in hydroxylation of heme O [J]. FEBS LETTERS, 2001, 492 (1-2) : 133 - +

[8] BECK EA, 1967, ACTA HAEMATOL-BASEL, V38, P1

[9] Bekri S, 2000, BLOOD, V96, P3256

[10] Iron overload in patients with sideroblastic anaemia is not related to the presence of the haemochromatosis Cys282Tyr and His63Asp mutations [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1999, 104 (01) : 97 - 99

[1] Mutation of a putative mitochondrial iron transporter gene (ABC7) in X-linked sideroblastic anemia and ataxia (XLSA/A) [J]. HUMAN MOLECULAR GENETICS, 1999, 8 (05) : 743 - 749

[2] AUTOSOMAL INHERITANCE OF SIDEROBLASTIC ANEMIA [J]. CLINICAL AND LABORATORY HAEMATOLOGY, 1988, 10 (03): : 347 - 353

[3] GAMMA-AMINOLEVULINIC ACID SYNTHETASE IN ERYTHROBLASTS OF PATIENTS WITH PYRIDOXINE-RESPONSIVE ANEMIA - HYPERCATABOLISM CAUSED BY THE INCREASED SUSCEPTIBILITY TO THE CONTROLLING PROTEASE [J]. JOURNAL OF CLINICAL INVESTIGATION, 1979, 64 (05) : 1196 - 1203

[4] ASHKENAZI A, 1973, PEDIATRICS, V52, P525

[5] Balduini CL, 1999, HAEMATOLOGICA, V84, P12

[6] A nuclear defect in the 4p16 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndrome [J]. JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (07) : 1570 - 1576

[7] Involvement of mitochondrial ferredoxin and Cox15p in hydroxylation of heme O [J]. FEBS LETTERS, 2001, 492 (1-2) : 133 - +

[8] BECK EA, 1967, ACTA HAEMATOL-BASEL, V38, P1

[9] Bekri S, 2000, BLOOD, V96, P3256

[10] Iron overload in patients with sideroblastic anaemia is not related to the presence of the haemochromatosis Cys282Tyr and His63Asp mutations [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1999, 104 (01) : 97 - 99