Mutation of a Putative Mitochondrial Iron Transporter Gene (ABC7) in X-Linked Sideroblastic Anemia and Ataxia (XLSA/A)
Rando Allikmets(Structural Genomics Consortium), David M. Koeller(University of Colorado Health), Nichole D Schueck(University of Colorado Health), Michael Dean(National Cancer Institute), Amy Hutchinson(National Institutes of Health), Wendy H. Raskind(Pacific Northwest Diabetes Research Institute)
Cited by 405
Related Papers
Genetic Restriction of HIV-1 Infection and Progression to AIDS by a Deletion Allele of the <i>CKR5</i> Structural Gene
|Science|1996|2.5k
A common haplotype in the complement regulatory gene factor H ( <i>HF1/CFH</i> ) predisposes individuals to age-related macular degeneration
|Proceedings of the National Academy of Sciences|2005|2k
The Human ATP-Binding Cassette (ABC) Transporter Superfamily
|Genome Research|2001|1.7k