PMS1 Polyclonal Antibody, 20ul Human Genome Knockout Libraries Mutations in this gene also

Mutations in this gene also cause autosomal recessive congenital alopecia and atrichia with papular lesions

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Certain mutations in KLKB1 cause prekallikrein deficiency

PMS1 Polyclonal Antibody, 20ul Human Genome Knockout Libraries Mutations in this gene alsoPMS1 encodes a protein belonging to the DNA mismatch repair mutL hexB family. PMS1 homolog 1, mismatch repair system component is thought to be involved in the repair of DNA mismatches, and it can form heterodimers with MLH1, a known DNA mismatch repair protein. Mutations in PMS1 cause hereditary nonpolyposis colorectal cancer type 3 (HNPCC3) either alone or in combination with mutations in other genes involved in the HNPCC phenotype, which is also