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RCN1 Rabbit Polyclonal Antibody, 100ul Deep Well Plates Mutations in MBTPS2 have been

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RCN1 Rabbit Polyclonal Antibody, 100ul Deep Well Plates Mutations in MBTPS2 have been

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Description

Mutations in MBTPS2 have been associated with ichthyosis follicularis with atrichia and photophobia (IFAP syndrome)

there is no evidence that the C-terminal half of the IgIII domain of this protein varies between three alternate forms

Heterozygous loss-of-function mutations in KLF1 result in the dominant In (Lu) blood phenotype

BUB3 encodes a protein involved in spindle checkpoint function

LAMA5 encodes one of the vertebrate laminin alpha chains

RCN1 Rabbit Polyclonal Antibody, 100ul Deep Well Plates Mutations in MBTPS2 have been

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