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BEAN1 Rabbit Polyclonal Antibody, 50ul sgRNA customized design loss of function mutations in

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BEAN1 Rabbit Polyclonal Antibody, 50ul sgRNA customized design loss of function mutations in100 copies of pentanucleotide repeats including a (TGGAA)n sequence) are associated with spinocerebellar ataxia type 31. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

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Description

loss of function mutations in the encoded protein have been shown to cause nonsyndromic progressive hearing loss

NBEAL2 contains one BEACH domain and five WD repeats

Members of this family are believed to be involved in embryogenesis

KRT18 encodes the type I intermediate filament chain keratin 18

BEAN1 Rabbit Polyclonal Antibody, 50ul sgRNA customized design loss of function mutations in100 copies of pentanucleotide repeats including a (TGGAA)n sequence) are associated with spinocerebellar ataxia type 31. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

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