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LRRT4 Rabbit Polyclonal Antibody, 20ul Fluorescent Staining Mutations in this gene are
LRRT4 Rabbit Polyclonal Antibody, 20ul Fluorescent Staining Mutations in this gene are
LRRT4 Rabbit Polyclonal Antibody, 20ul Fluorescent Staining Mutations in this gene are
LRRT4 Rabbit Polyclonal Antibody, 20ul Fluorescent Staining Mutations in this gene are

LRRT4 Rabbit Polyclonal Antibody, 20ul Fluorescent Staining Mutations in this gene are

SKU: 9433705750

4.1
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LRRT4 Rabbit Polyclonal Antibody, 20ul Fluorescent Staining Mutations in this gene are

Store: avramcheva.com · Domain: avramcheva.com

Description

Mutations in this gene are associated with achromatopsia (rod monochromacy) and color blindness

This gene is co-transcribed with the U65 snoRNA

Defects in this gene are cause of an autosomal recessive cutis laxa syndrome

which contain multiple tyrosine residues and putative SH2 binding sites

which is the primary mechanism for the removal of cholesterol from the body

LRRT4 Rabbit Polyclonal Antibody, 20ul Fluorescent Staining Mutations in this gene are

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