Single nucleotide polymorphism in a commonly utilized LAMB3 primer sequence: implications for mutation detection and haplotype analysis in junctional epidermolysis bullosa.

Lu Liu; Yew Sing Choy; Vesarat Wessagowit; Linda Ozoemena; Patricia J C Dopping-Hepenstal; Hiva Fassihi; John A McGrath

doi:10.1016/j.jdermsci.2006.05.009

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Single nucleotide polymorphism in a commonly utilized LAMB3 primer sequence: implications for mutation detection and haplotype analysis in junctional epidermolysis bullosa.

Lu Liu·Yew Sing Choy·Vesarat Wessagowit·Linda Ozoemena·Patricia J C Dopping-Hepenstal·Hiva Fassihi·John A McGrath

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Base Sequence Cell Adhesion Molecules DNA Mutational Analysis DNA Primers Epidermolysis Bullosa, Junctional Female Haplotypes Humans Infant, Newborn Male Molecular Sequence Data Polymorphism, Single Nucleotide Kalinin Case Reports Letter Research Support, Non-U.S. Gov't

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Lu Liu, Yew Sing Choy, Vesarat Wessagowit, Linda Ozoemena, Patricia J C Dopping-Hepenstal, Hiva Fassihi, John A McGrath. 2006-06-30. Single nucleotide polymorphism in a commonly utilized LAMB3 primer sequence: implications for mutation detection and haplotype analysis in junctional epidermolysis bullosa.. https://doi.org/10.1016/j.jdermsci.2006.05.009

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