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Mutations in EXPH5 underlie a rare subtype of autosomal recessive epidermolysis bullosa simplex
Mutations in EXPH5 underlie a rare subtype of autosomal recessive epidermolysis bullosa simplex
2016
Ellie Rashidghamat
Linda Ozoemena
Lin Liu
John A. McGrath
Anna E. Martinez
Jemima E. Mellerio
Keywords:
Dermatology
Epidermolysis bullosa simplex
Cancer research
Dominance (genetics)
Medicine
Pathology
Correction
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