Title : Recurrent R156H mutation of KRT10 in a Japanese family with bullous congenital ichthyosiform erythroderma.

Pub. Date : 2000 Jul

PMID : 11204523






1 Functional Relationships(s)
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Protein Name
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1 The substitution of arginine (R) to histidine (H) at amino acid residue 156 (R156H) of coiled 1A region is one of the most frequent mutations of KRT10. Histidine keratin 10 Homo sapiens