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SNX8 Rabbit Polyclonal Antibody, 20ul Reagent Reservoirs Mutations in this gene are

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SNX8 Rabbit Polyclonal Antibody, 20ul Reagent Reservoirs Mutations in this gene are

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Description

Mutations in this gene are associated with epidermolysis bullosa with pyloric atresia

Defects in TRPS1 are a cause of tricho-rhino-phalangeal syndrome (TRPS) types I-III

Members of the SOX family of transcription factors are characterized by the presence of a DNA-binding high mobility group (HMG) domain

breast cancers progress to become anti-estrogen resistant

Alternatively spliced transcript variants have been found for ELOVL5

SNX8 Rabbit Polyclonal Antibody, 20ul Reagent Reservoirs Mutations in this gene are

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