Biallelic KRT5 mutations in autosomal recessive epidermolysis bullosa simplex, including a complete human keratin 5 “knock-out”
Keyword(s):
Keyword(s):
1995 ◽
Vol 4
(10)
◽
pp. 1999-2000
◽
2013 ◽
Vol 39
(1)
◽
pp. 80-81
◽
2013 ◽
Vol 23
(2)
◽
pp. 267-269
◽
Keyword(s):
1997 ◽
Vol 108
(5)
◽
pp. 809-810
◽