Beemer–Langer syndrome is a ciliopathy due to biallelic mutations in IFT122

Volume: 173, Issue: 5, Pages: 1186 - 1189
Published: Mar 28, 2017
Abstract
Since most short-rib polydactyly phenotypes are due to genes involved with biogenesis and maintenance of the primary cilium, this group of skeletal dysplasias was recently designated as ciliopathies with major skeletal involvement. Beemer-Langer syndrome or short-rib polydactyly type IV, was first described in 1983, and has, thus far, remained without a defined molecular basis. The most recent classification of the skeletal dysplasias referred...
Paper Details
Title
Beemer–Langer syndrome is a ciliopathy due to biallelic mutations in IFT122
Published Date
Mar 28, 2017
Volume
173
Issue
5
Pages
1186 - 1189
Citation AnalysisPro
  • Scinapse’s Top 10 Citation Journals & Affiliations graph reveals the quality and authenticity of citations received by a paper.
  • Discover whether citations have been inflated due to self-citations, or if citations include institutional bias.