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Lamin B1 Polyclonal Antibody, 50ul[BT-AP04935] Biomatrix Mutations in this gene cause

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Lamin B1 Polyclonal Antibody, 50ul[BT-AP04935] Biomatrix Mutations in this gene causeLMNB1 encodes one of the two B type lamin proteins and is a component of the nuclear lamina. A duplication of LMNB1 is associated with autosomal dominant adult onset leukodystrophy (ADLD). Alternative splicing results in multiple transcript variants.

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Description

Mutations in this gene cause a multiple congenital anomaly syndrome in human patients

Mutations in this gene have been associated with adducted thumb-clubfoot syndrome

Multiple transcript variants encoding several different isoforms have been found for NOP56

which converts inositol 1

Lamin B1 Polyclonal Antibody, 50ul[BT-AP04935] Biomatrix Mutations in this gene causeLMNB1 encodes one of the two B type lamin proteins and is a component of the nuclear lamina. A duplication of LMNB1 is associated with autosomal dominant adult onset leukodystrophy (ADLD). Alternative splicing results in multiple transcript variants.

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