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CNPY4 Rabbit Polyclonal Antibody, 50ul sgRNA Library Construction Mutations in this gene cause
CNPY4 Rabbit Polyclonal Antibody, 50ul sgRNA Library Construction Mutations in this gene cause
CNPY4 Rabbit Polyclonal Antibody, 50ul sgRNA Library Construction Mutations in this gene cause
CNPY4 Rabbit Polyclonal Antibody, 50ul sgRNA Library Construction Mutations in this gene cause

CNPY4 Rabbit Polyclonal Antibody, 50ul sgRNA Library Construction Mutations in this gene cause

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CNPY4 Rabbit Polyclonal Antibody, 50ul sgRNA Library Construction Mutations in this gene cause

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Description

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

These proteins are putative RNA helicases

leading to compete with ITCHs substrates and impairing ubiquitination of substrates

These complexes are found in some cilia and are assembled in the cytoplasm prior to transport for cilia formation

It is found associated with high density lipoproteins and to a lesser extent with low density lipoproteins and triglyceride-rich lipoproteins

CNPY4 Rabbit Polyclonal Antibody, 50ul sgRNA Library Construction Mutations in this gene cause

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