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ST3L2 Rabbit Polyclonal Antibody, 100ul Recombinant Ab Production Defects in CLDN19 are the

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ST3L2 Rabbit Polyclonal Antibody, 100ul Recombinant Ab Production Defects in CLDN19 are the

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Description

Defects in CLDN19 are the cause of hypomagnesemia renal with ocular involvement (HOMGO)

a region which contains several major histocompatibility complex (MHC) genes

Experience secure and efficient centrifugation with our 1

This gene encodes a member of a family of proteins that contain coiled-coil domains and may form hetero- or homomers

ST3L2 Rabbit Polyclonal Antibody, 100ul Recombinant Ab Production Defects in CLDN19 are the

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