All individuals with variants in gene SCP2

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AscendingIndividual ID     

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Owner     
00398753 721 PubMed: Ferese 2021 2-generation family, 1 affected M - Italy - >59y - - - CMS8, LKDMN Peripheral neuropathy (HP:0009830), Decreased nerve conduction velocity (HP:0000762), Bradyphrenia (HP:0031843), Cognitive impairment (HP:0100543), Paresthesia (HP:0003401) 1 1 Yvet den Hartog
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