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VHLL Rabbit Polyclonal Antibody, 100ul Transporters Mutations in this gene are

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VHLL Rabbit Polyclonal Antibody, 100ul Transporters Mutations in this gene are

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Description

Mutations in this gene are also the cause of Noonan syndrome-like disorder

Specific mutations in DYSF have been shown to cause autosomal recessive limb girdle muscular dystrophy type 2B (LGMD2B) as well as Miyoshi myopathy

a smooth muscle actin found in enteric tissues

The protein encoded by this gene can interact with PSD-95 through its guanylate kinase domain and may be involved in clustering PSD-95 in the postsynaptic density region

Multiple alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported

VHLL Rabbit Polyclonal Antibody, 100ul Transporters Mutations in this gene are

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