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

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

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

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Description

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

Among its related pathways are C-MYC pathway and Regulation of Wnt-mediated beta catenin signaling and target gene transcription

Lecithin retinol acyltransferase encoded by LRAT localizes to the endoplasmic reticulum

Defects in SLC6A11 may result in epilepsy

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

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

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