MNX1 Polyclonal Antibody, 50ul Sealing Film The chromosome 22 breakpoint for
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MNX1 Polyclonal Antibody, 50ul Sealing Film The chromosome 22 breakpoint forThis gene encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
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