potassium two pore domain channel subfamily K member 9
OMIM: 605874, Gene2Phenotype
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KCNK9 in Mendeliome
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review | MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed) |
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KCNK9 in Intellectual disability syndromic and non-syndromic
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review | MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed) |
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Phenotypes
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KCNK9 in Imprinting disorders
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review | MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed) |
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Phenotypes
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