LAMB3 gene mutation

Clinical significance

• defects in LAMB3 are a cause of
  • epidermolysis bullosa junctional Herlitz type
  • generalized atrophic benign epidermolysis bullosa
  • amelogenesis imperfecta type 1A

More general terms

• gene mutation testing; gene mutation analysis

Additional terms

• laminin beta-3 (nicein alpha, kalinin B1 chain, BM600, laminin B1k, LAMB3 LAMNB1)