All individuals with variants in gene AP5M1

3 entries on 1 page. Showing entries 1 - 3.
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AscendingIndividual ID     

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00464726 Fam15Pat18 PubMed: Kaminska 2025 3-generation family, 1 affected, unaffected heterozygous carrier parents M - Switzerland - - - - - macular dystrophy macular dystrophy; reduced central vision; maculopathy with atrophy and deposits; mild intellectual disability 1 1 Johan den Dunnen
00464727 Fam16Pat19 PubMed: Kaminska 2025 2-generation family, 1 affected, unaffected heterozygous carrier parents M - Belgium - - - - - macular dystrophy macular dystrophy; Parkinson symptoms; extensive central chorioretinal atrophy; parkinsonism; type 2 diabetes; ischemic stroke 1 1 Johan den Dunnen
00464728 Fam17Pat20 PubMed: Kaminska 2025 2-generation family, 1 affected, unaffected heterozygous carrier parents M - Germany - - - - - macular dystrophy macular dystrophy; central vision loss; extensive central chorioretinal atrophy; no neurological symptoms; myocardial infarction; multiple allergies; chronic anal fistulas 1 1 Johan den Dunnen
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