TM4SF10 gene sequencing in XLMR patients identifies common polymorphisms but no disease-associated mutation
<p>Abstract</p> <p>Background</p> <p>The TM4SF10 gene encodes a putative four-transmembrane domains protein of unknown function termed Brain Cell Membrane Protein 1 (BCMP1), and is abundantly expressed in the brain. This gene is located on the short arm of human chromos...
Main Authors: | Holinski-Feder Elke, Abramowicz Marc J, Gecz Jozef, Kooy Frank, Christophe-Hobertus Christiane, Schwartz Charles, Christophe Daniel |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2004-09-01
|
Series: | BMC Medical Genetics |
Online Access: | http://www.biomedcentral.com/1471-2350/5/22 |
Similar Items
-
XLMR in MRX families 29, 32, 33 and 38 results from the dup24 mutation in the ARX (Aristaless related homeobox) gene
by: MacMillan Andrée, et al.
Published: (2005-04-01) -
The role of epigenetic factors in the pathogenesis of familial X-linked mental retardation (XLMR)
by: Carvill, Gemma
Published: (2014) -
Contribution à l'étude du contrôle transcriptionnel dans la thyroïde
by: Christophe-Hobertus, Christiane
Published: (2002) -
Down-regulation of TM4SF is associated with the metastatic potential of gastric carcinoma TM4SF members in gastric carcinoma
by: Zhu Guanbao, et al.
Published: (2011-04-01) -
The FTO, PNPLA3 and TM6SF2 Gene Polymorphisms and Genetic Predisposition to NAFLD in Yakut Population
by: Aleksandra T. Diakonova, et al.
Published: (2021-03-01)