X-linked ataxias
Author:
Publisher
Elsevier
Reference130 articles.
1. Mutation of a putative mitochondrial iron transporter gene (ABC7) in X-linked sideroblastic anemia and ataxia (XLSA/A);Allikmets;Hum Mol Genet,1999
2. Novel intragenic deletion in OPHN1 in a family causing XLMR with cerebellar hypoplasia and distinctive facial appearance;Al-Owain;Clin Genet,2011
3. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat Genet,1999
4. The Opitz syndrome gene product MID1 assembles a microtubule-associated ribonucleoprotein complex;Aranda-Orgillés;Hum Genet,2008
5. Locomotor and oculomotor impairment associated with cerebellar dysgenesis in Zic3-deficient (bent tail) mutant mice;Aruga;Eur J Neurosci,2004
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