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MFS11 Rabbit Polyclonal Antibody, 50ul Monoclonal Antibodies Mutations in this gene are

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MFS11 Rabbit Polyclonal Antibody, 50ul Monoclonal Antibodies Mutations in this gene are

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Description

Mutations in this gene are associated with osteoarthritis in humans

DDX20 encodes a DEAD box protein

a calcium-binding EF hand and a divergent SH2 domain

Defects in CLCN7 are the cause of osteopetrosis autosomal recessive type 4 (OPTB4)

MIM 606197) and plays a role in an early step of neural development (Bellefroid et al

MFS11 Rabbit Polyclonal Antibody, 50ul Monoclonal Antibodies Mutations in this gene are

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