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LAMB3 gene mutation
Clinical significance:
- defects in LAMB3 are a cause of
a) epidermolysis bullosa junctional Herlitz type
b) generalized atrophic benign epidermolysis bullosa
c) amelogenesis imperfecta type 1A
Related
laminin beta-3 (nicein alpha, kalinin B1 chain, BM600, laminin B1k, LAMB3 LAMNB1)
General
gene mutation testing; gene mutation analysis
References
Loinc