Alopecia, Neurological Defects, and Endocrinopathy Syndrome Caused by Decreased Expression of RBM28, a Nucleolar Protein Associated with Ribosome Biogenesis
Open Access
- 24 April 2008
- journal article
- research article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 82 (5) , 1114-1121
- https://doi.org/10.1016/j.ajhg.2008.03.014
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Dystonia in the Woodhouse Sakati syndrome: A new family and literature reviewMovement Disorders, 2008
- Homeodomain-Mediated β-Catenin-Dependent Switching Events Dictate Cell-Lineage DeterminationCell, 2006
- Mendelian disorders deserve more attentionNature Reviews Genetics, 2006
- Prp43p Is a DEAH-Box Spliceosome Disassembly Factor Essential for Ribosome BiogenesisMolecular and Cellular Biology, 2006
- Johnson‐McMillin syndrome: Report of a new case with novel featuresBirth Defects Research Part A: Clinical and Molecular Teratology, 2005
- Nucleolar proteome dynamicsNature, 2005
- Genetic hair and nail disordersClinics in Dermatology, 2005
- β-Catenin Controls Hair Follicle Morphogenesis and Stem Cell Differentiation in the SkinCell, 2001
- The Yeast Nucleolar Protein Nop4p Contains Four RNA Recognition Motifs Necessary for Ribosome BiogenesisPublished by Elsevier ,1997
- Progressive extrapyramidal disorder with primary hypogonadism and alopecia in sibs: A new syndrome?American Journal of Medical Genetics, 1996