Disease: Anemia sideroblastic and spinocerebellar ataxia
- Abcb7, the gene responsible for X-linked sideroblastic anemia with ataxia, is essential for hematopoiesis
- Chromosomal abnormalities and their specificity in human neoplasms: an assessment of recent observations by banding techniques
- Cloning and chromosomal mapping of a novel ABC transporter gene (hABC7), a candidate for X-linked sideroblastic anemia with spinocerebellar ataxia
- Cytogenetics and hemopathies
- Expression, purification and microscopic characterization of human ATP-binding cassette sub-family B member 7 protein
- Hereditary Ataxia: A Focus on Heme Metabolism and Fe-S Cluster Biogenesis
- Hereditary sideroblastic anaemia and ataxia: an X linked recessive disorder
- Spinocerebellar ataxias due to mitochondrial defects
- The idic(X)(q13) in myeloid malignancies: breakpoint clustering in segmental duplications and association with TET2 mutations
- Whole-genome sequencing identifies a novel ABCB7 gene mutation for X-linked congenital cerebellar ataxia in a large family of Mongolian ancestry
- X-Linked Sideroblastic Anemia and Ataxia - RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY
- X-Linked Sideroblastic Anemia and Ataxia – RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY