Maternal Uniparental Disomy of Chromosome 1 with Reduction to Homozygosity of the LAMB3 Locus in a Patient with Herlitz Junctional Epidermolysis Bullosa
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics
Reference41 articles.
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3. A novel homozygous nonsense mutation in the LAMC2 gene in patients with the Herlitz junctional epidermolysis bullosa;Baudoin;Hum Mol Genet,1994
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