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PNM6C Rabbit Polyclonal Antibody, 20ul Primary Antibodies Mutations in this gene are

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PNM6C Rabbit Polyclonal Antibody, 20ul Primary Antibodies Mutations in this gene are

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Description

Mutations in this gene are associated with platelet-type bleeding disorders

The protein encoded also exhibits antimicrobial activity against bacteria

Represses basal transcription activity from target promoters (By similarity)

Mutations in TUBB3 are the cause of congenital fibrosis of the extraocular muscles type 3

Activation of T cells through the T cell receptor (TCR) results in tyrosine phosphorylation of CD5

PNM6C Rabbit Polyclonal Antibody, 20ul Primary Antibodies Mutations in this gene are

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