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Mutations in IFT80 cause SRPS Type IV. Report of two families and review.

Varoona BizaouiCéline HuberEva KohautJoelle RoumeMaryse BonnièreTania Attié-BitachValérie Cormier-Daire
Published in: American journal of medical genetics. Part A (2019)
We report novel causative mutations in the IFT80 gene identified in four fetuses from two unrelated families with Beemer-Langer syndrome (BLS) or BLS-like phenotypes. We discuss the implication of the IFT80 gene in ciliopathies, and its diagnostic value for BLS among other SRPS.
Keyphrases
  • copy number
  • genome wide
  • genome wide identification
  • case report
  • dna methylation
  • genome wide analysis