Login / Signup

Novel autosomal recessive LAMA3 and PLEC variants underlie junctional epidermolysis bullosa generalized intermediate and epidermolysis bullosa simplex with muscular dystrophy in two consanguineous families.

F AhmadK ShahM UmairA Jannull IrfanullahS KhanD MuhammadS BasitS M WakilK RamzanWasim Ahmad
Published in: Clinical and experimental dermatology (2018)
Keyphrases
  • muscular dystrophy
  • duchenne muscular dystrophy
  • copy number
  • autism spectrum disorder