Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataract
- 3 September 2006
- journal article
- research article
- Published by Springer Science and Business Media LLC in Nature Genetics
- Vol. 38 (10), 1111-1113
- https://doi.org/10.1038/ng1870
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Wnt signaling regulates the sequential onset of neurogenesis and gliogenesis via induction of BMPsGenes to Cells, 2005
- Wnt signaling controls the timing of oligodendrocyte development in the spinal cordDevelopmental Biology, 2005
- Mutations in the Gene Encoding Gap Junction Protein α12 (Connexin 46.6) Cause Pelizaeus-Merzbacher–Like DiseaseAmerican Journal of Human Genetics, 2004
- The latest on leukodystrophiesCurrent Opinion in Neurology, 2004
- A role for Wnt/β-catenin signaling in lens epithelial differentiationDevelopmental Biology, 2003
- Defining and Categorizing Leukoencephalopathies of Unknown Origin: MR Imaging ApproachRadiology, 1999
- Connexin46 Mutations in Autosomal Dominant Congenital CataractAmerican Journal of Human Genetics, 1999
- A Missense Mutation in the Human Connexin50 Gene (GJA8) Underlies Autosomal Dominant “Zonular Pulverulent” Cataract, on Chromosome 1qAmerican Journal of Human Genetics, 1998
- EEA1, an Early Endosome-Associated Protein.Published by Elsevier BV ,1995
- Connexin Mutations in X-Linked Charcot-Marie-Tooth DiseaseScience, 1993