Disorders of Heme Biosynthesis: X-Linked Sideroblastic Anemia and the Porphyrias
The human counterpart of zebrafish shiraz shows sideroblastic-like microcytic anemia and iron overload.
A new syndrome of refractory sideroblastic anemia with vacuolization of marrow precursors and exocrine pancreatic dysfunction.
Mitochondrial ferritin expression in erythroid cells from patients with sideroblastic anemia
Positional cloning of the zebrafish sauternes gene: a model for congenital sideroblastic anaemia
Mitochondrial myopathy and sideroblastic anemia (MLASA): missense mutation in the pseudouridine synthase 1 (PUS1) gene is associated...
Missense Mutation in Pseudouridine Synthase 1 () Causes Mitochondrial Myopathy and Sideroblastic Anemia (MLASA)
Mutation of a putative mitochondrial iron transporter gene (ABC7) in X-linked sideroblastic anemia and ataxia (XLSA/A).
Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia
Mutation of the Mitochondrial Tyrosyl-tRNA Synthetase Gene, YARS2, Causes Myopathy, Lactic Acidosis, and Sideroblastic Anemia—MLASA...
