TM4SF10 gene sequencing in XLMR patients identifies common polymorphisms but no disease-associated mutation-Reference-Cited by-同舟云学术

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TM4SF10 gene sequencing in XLMR patients identifies common polymorphisms but no disease-associated mutation

Published:2004-09-02 Issue:1 Volume:5 Page:
ISSN:1471-2350
Container-title:BMC Medical Genetics
language:en
Short-container-title:BMC Med Genet

Author:

Christophe-Hobertus Christiane,Kooy Frank,Gecz Jozef,Abramowicz Marc J,Holinski-Feder Elke,Schwartz Charles,Christophe Daniel

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1186/1471-2350-5-22.pdf

Reference16 articles.

1. Christophe-Hobertus C, Szpirer C, Guyon R, Christophe D: Identification of the gene encoding Brain Cell Membrane Protein 1 (BCMP1), a putative four-transmembrane protein distantly related to the Peripheral Myelin Protein 22 / Epithelial Membrane Proteins and the Claudins. BMC Genomics. 2001, 2: 3-10.1186/1471-2164-2-3.

2. Simske JS, Köppen M, Sims P, Hodgkin J, Yonkof A, Hardin J: The cell junction protein VAB-9 regulates adhesion and epidermal morphology in C. elegans. Nature Cell Biol. 2003, 5: 619-625. 10.1038/ncb1002.

3. SAGEmap. [ http://www.ncbi.nlm.nih.gov/SAGE/ ]

4. Zemni R, Bienvenu T, Vinet MC, Sefiani A, Carrié A, Billuart P, McDonell N, Couvert P, Francis F, Chafey P, Fauchereau F, Friocourt G, des Portes V, Cardona A, Frints S, Meindl A, Brandau O, Ronce N, Moraine C, van Bokhoven H, Ropers HH, Sudbrak R, Kahn A, Fryns JP, Beldjord C, Chelly J: A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation. Nature Genet. 2000, 24: 167-170. 10.1038/72829.

5. Abidi FE, Holinski-Feder E, Rittinger O, Kooy F, Lubs HA, Stevenson RE, Schwartz CE: A novel 2 bp deletion in the TM4SF2 gene is associated with MRX58. J Med Genet. 2002, 39: 430-433. 10.1136/jmg.39.6.430.

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