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TMC7 Polyclonal Antibody, 50ul Cell fragmentation and collection Diseases associated with SLC5A6 include

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TMC7 Polyclonal Antibody, 50ul Cell fragmentation and collection Diseases associated with SLC5A6 include

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Description

Diseases associated with SLC5A6 include thiamine metabolism dysfunction syndrome 2 and urinary tract obstruction

Two transcript variants encoding different isoforms have been found for PYCARD

RAD51 family members are evolutionarily conserved proteins essential for DNA repair by homologous recombination

Mutations in this gene cause nocturnal frontal lobe epilepsy type 1

This gene encodes a member of the septin family of cytoskeletal proteins with GTPase activity

TMC7 Polyclonal Antibody, 50ul Cell fragmentation and collection Diseases associated with SLC5A6 include

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