Homozygous alpha6 integrin mutation in junctional epidermolysis bullosa with congenital duodenal atresia.

Pulkkinen, L

Homozygous alpha6 integrin mutation in junctional epidermolysis bullosa with congenital duodenal atresia. [electronic resource] - Human molecular genetics May 1997 - 669-74 p. digital

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.

0964-6906

10.1093/hmg/6.5.669 doi


Antigens, CD--genetics
Blister
Chromosome Mapping
Chromosomes, Human, Pair 2
Duodenal Obstruction--congenital
Epidermolysis Bullosa, Junctional--complications
Exons
Female
Homozygote
Humans
Infant, Newborn
Integrin alpha6
Introns
Male
Molecular Sequence Data
Mutation
Pedigree
Pregnancy