Recurrent intragenic deletion mutation in desmoglein 4 gene underlies autosomal recessive hypotrichosis in two Pakistani families of Balochi and Sindhi origins.
John, Peter
Recurrent intragenic deletion mutation in desmoglein 4 gene underlies autosomal recessive hypotrichosis in two Pakistani families of Balochi and Sindhi origins. [electronic resource] - Archives of dermatological research Aug 2006 - 135-7 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0340-3696
10.1007/s00403-006-0671-3 doi
Base Sequence
Desmogleins--genetics
Female
Genes, Recessive
Humans
Hypotrichosis--genetics
Male
Pakistan
Pedigree
Sequence Deletion
Recurrent intragenic deletion mutation in desmoglein 4 gene underlies autosomal recessive hypotrichosis in two Pakistani families of Balochi and Sindhi origins. [electronic resource] - Archives of dermatological research Aug 2006 - 135-7 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0340-3696
10.1007/s00403-006-0671-3 doi
Base Sequence
Desmogleins--genetics
Female
Genes, Recessive
Humans
Hypotrichosis--genetics
Male
Pakistan
Pedigree
Sequence Deletion