All individuals with variants in gene GRIN2C

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00458161 Fam6PatII1 PubMed: Jurkute 2021 2-generation family, 1 affected, unaffected non carrier parents M - United Kingdom (Great Britain) - - - - - NDD see paper; ..., childhood onset; >7y-optic atrophy; no hearing impairment; ataxia/balance problems (childhood); sensory neuropathy (childhood); no motor neuropathy; no dizziness; no tremor; 7y-no retinal dystrophy; no macula edema; no retinal vessels attenuation; 18y-cataract; >7y-nystagmus; no squint 1 1 Johan den Dunnen
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