All individuals with variants in gene HACE1

2 entries on 1 page. Showing entries 1 - 2.
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AscendingIndividual ID     

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Owner     
00415277 32 PubMed: Alfares 2018 - F - - - - - - - retinal disease OMIM: 616756; intellectual disability, spasticity, and neurogenic bladder 1 1 LOVD
00444511 Pat13 PubMed: Riquin 2023 patient M - France - - - - - NDD Myoclonic epilepsy, encephalopathy, axial hypotonia, languange acquisition then regression, cortical atrophy on cerebral MRI, myelinisation delay, thin corpus callosum 2 1 Johan den Dunnen
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