Lack of evidence of WNT3A as a candidate gene for congenital vertebral malformations Academic Article uri icon

Overview

MeSH Major

  • Magnetic Resonance Imaging
  • Osteogenesis Imperfecta
  • Skin

abstract

  • These data suggest that WNT3A does not contribute towards the development of congenital vertebral malformations. Factors such as phenotypic and genetic heterogeneity may underlie our inability to detect mutations in WNT3A in our patient sample.

publication date

  • September 23, 2007

Research

keywords

  • Academic Article

Identity

Language

  • eng

PubMed Central ID

  • PMC2064903

Digital Object Identifier (DOI)

  • 10.1186/1748-7161-2-13

PubMed ID

  • 17888180

Additional Document Info

start page

  • 13

volume

  • 2

number

  • 1