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SH3L2 Polyclonal Antibody, 50ul 3D Culture Mutations in this gene are

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SH3L2 Polyclonal Antibody, 50ul 3D Culture Mutations in this gene are

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Description

Mutations in this gene are associated with hypotrichosis with juvenile macular dystrophy and ectodermal dysplasia

An important paralog of this gene is PTGFRN

This protein has an amino terminal RING domain which is followed by four zinc-finger motifs

1998 [PubMed: 9616133])

Also present in thymus and bone marrow and low levels observed in prostate

SH3L2 Polyclonal Antibody, 50ul 3D Culture Mutations in this gene are

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