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KTN1 Rabbit Polyclonal Antibody, 50ul NGS Oligos Mutations in TNNI3 cause familial

SKU: 59890589459

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KTN1 Rabbit Polyclonal Antibody, 50ul NGS Oligos Mutations in TNNI3 cause familial

Store: aashay.com.au · Domain: aashay.com.au

Description

Mutations in TNNI3 cause familial hypertrophic cardiomyopathy type 7 (CMH7) and familial restrictive cardiomyopathy (RCM)

Pseudogenes of this gene are found on chromosomes 5

In mouse this protein may be involved in fibroblast growth factor regulated growth control

Alternately-spliced IL2RA mRNAs have been isolated

they are transmembrane proteins containing 2 immunoglobulin (Ig)-like domains and 2 type I thrombospondin motifs in the extracellular region

KTN1 Rabbit Polyclonal Antibody, 50ul NGS Oligos Mutations in TNNI3 cause familial

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