X61028[Secondary Source ID] - Search Results

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Allelic variations of human keratins K4 and K5 provide polymorphic markers within the type II keratin gene cluster on chromosome 12.

Wanner R, Förster HH, Tilmans I, Mischke D. Wanner R, et al. J Invest Dermatol. 1993 Jun;100(6):735-41. doi: 10.1111/1523-1747.ep12475671. J Invest Dermatol. 1993. PMID: 7684424 Free article.

Dominant and recessive compound heterozygous mutations in epidermolysis bullosa simplex demonstrate the role of the stutter region in keratin intermediate filament assembly.

Yasukawa K, Sawamura D, McMillan JR, Nakamura H, Shimizu H. Yasukawa K, et al. J Biol Chem. 2002 Jun 28;277(26):23670-4. doi: 10.1074/jbc.M200974200. Epub 2002 Apr 24. J Biol Chem. 2002. PMID: 11973334 Free article.

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