Novel autosomal recessive LAMA3 and PLEC variants underlie junctional epidermolysis bullosa generalized intermediate and epidermolysis bullosa simplex with muscular dystrophy in two consanguineous families
Clinical and Experimental Dermatology, EarlyView.
Source: Clinical And Experimental Dermatology - Category: Dermatology Authors: F. Ahmad
,
K. Shah
,
M. Umair
,
A. Jan
,
Irfanullah
,
S. Khan
,
D. Muhammad
,
S. Basit
,
S. M. Wakil
,
K. Ramzan
,
W. Ahmad Source Type: research
More News: Dermatology | Epidermolysis Bullosa | Muscular Dystrophy | Reflex Sympathetic Dystrophy | Skin