| Literature DB >> 8012393 |
L Pulkkinen1, A M Christiano, T Airenne, H Haakana, K Tryggvason, J Uitto.
Abstract
Junctional epidermolysis bullosa (JEB) is an autosomal recessive disorder characterized by blister formation within the dermal-epidermal basement membrane. Genes for the lamina lucida protein, kalinin/laminin 5, have been proposed as candidates for some forms of JEB, based on immunofluorescence analysis recognizing kalinin epitopes. We studied the cDNA of laminin gamma 2 chain for mutations in JEB using heteroduplex analysis. One patient showed a homozygous splice site mutation while another was heterozygous for a deletion-insertion, resulting in a premature termination codon in one allele. Our data implicate mutations in the laminin gamma 2 chain gene (LAMC2) in some forms of JEB.Entities:
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Year: 1994 PMID: 8012393 DOI: 10.1038/ng0394-293
Source DB: PubMed Journal: Nat Genet ISSN: 1061-4036 Impact factor: 38.330