Login / Signup

A Novel Compound Heterozygous Variant in the LLS gene is Associated with Non-Syndromic Hypotrichosis.

Fanny Morice-PicardPierre-Louis LanvinEulalie LasseauxFranck BoraleviChristine LabrèzeLouis Lebreton
Published in: Clinical and experimental dermatology (2023)
Keyphrases
  • intellectual disability
  • early onset
  • copy number
  • genome wide
  • genome wide identification
  • autism spectrum disorder