Neuronally-expressed necdin gene: an imprinted candidate gene in Prader-Willi syndrome
- 22 November 1997
- journal article
- Published by Elsevier in The Lancet
- Vol. 350 (9090) , 1520-1521
- https://doi.org/10.1016/s0140-6736(05)63943-8
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- The Necdin Gene is Deleted in Prader-Willi Syndrome and is Imprinted in Human and MouseHuman Molecular Genetics, 1997
- The E6–AP Ubiquitin–Protein Ligase (UBE3A) Gene Is Localized within a Narrowed Angelman Syndrome Critical RegionGenome Research, 1997
- Arrest of Cell Growth by Necdin, a Nuclear-Protein Expressed in Postmitotic NeuronsBiochemical and Biophysical Research Communications, 1995
- Expression of necdin, an embryonal carcinoma-derived nuclear protein, in developing mouse brainDevelopmental Brain Research, 1992
- A novel brain-specific mRNA encoding nuclear protein (necdin) expressed in neurally differentiated embryonal carcinoma cellsBiochemical and Biophysical Research Communications, 1991