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Oligodontia Is Caused by Mutation in LTBP3, the Gene Encoding Latent TGF-β Binding Protein 3

Authors :
Benjamin A. Alman
Irina Vitcu
Abdul Noor
John B. Vincent
Christian Windpassinger
Mahwish Khalid
Muhammad Rafiq
Mahmood Nasir Malik
Marija Orlic
Muhammad Ayub
Source :
The American Journal of Human Genetics. (4):519-523
Publisher :
The American Society of Human Genetics. Published by Elsevier Inc.

Abstract

We have identified a consanguineous Pakistani family where oligodontia is inherited along with short stature in an autosomal-recessive fashion. Increased bone density was present in the spine and at the base of the skull. Using high-density single-nucleotide polymorphism microarrays for homozygosity mapping, we identified a 28 Mb homozygous stretch shared between affected individuals on chromosome 11q13. Screening selected candidate genes within this region, we identified a homozygous nonsense mutation, Y774X, within LTBP3, the gene for the latent TGF-beta binding protein 3, an extracellular matrix protein believed to be required for osteoclast function.

Details

Language :
English
ISSN :
00029297
Issue :
4
Database :
OpenAIRE
Journal :
The American Journal of Human Genetics
Accession number :
edsair.doi.dedup.....fa9c558c56936ff48e222c8a6a998f47
Full Text :
https://doi.org/10.1016/j.ajhg.2009.03.007