Title : R156C mutation of keratin 10 causes mild form of epidermolytic hyperkeratosis.

Pub. Date : 2007 Aug

PMID : 17683385






1 Functional Relationships(s)
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1 Following direct sequencing, we found a single nucleotide substitution in one allele at the residue position 466 of the 1A rod domain segment (CGC to TGC, arginine to cysteine; R156C) in keratin 10. Arginine keratin 10 Homo sapiens