All individuals with variants in gene UFC1

8 entries on 1 page. Showing entries 1 - 8.
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AscendingIndividual ID     

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VIP     

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Owner     
00177066 76366 PubMed: Nahorski 2018 2-generation family, 1 affected, unaffected heterozygous carrier parents M yes Switzerland - - - - - EE HP:0007325 HP:0001285 HP:0005348 HP:0002705 HP:0010804 HP:0000293 HP:0011800 HP:0009748 HP:0009803 1 1 Anaïs Begemann
00179399 29868776-Fam1Pats PubMed: Nahorski 2018 4-generation family, 3 affected sisters, unaffected heterozygous carrier parents/relatives F yes Saudi Arabia - - - - - EE see paper; ..., severe early infantile encephalopathy, progressive microcephaly, axial hypotonia, appendicular hypertonia, refractory epilepsy 1 3 Johan den Dunnen
00179400 29868777-Fam2Pats PubMed: Nahorski 2018 4-generation family, 2 affecteds (2F), unaffected heterozygous carrier parents/relatives F yes Saudi Arabia - - - - - EE see paper; ..., severe early infantile encephalopathy, progressive microcephaly, axial hypotonia, appendicular hypertonia, refractory epilepsy 1 2 Johan den Dunnen
00179401 29868778-Fam2Pats PubMed: Nahorski 2018 3-generation family, 2 affecteds (2F), unaffected heterozygous carrier parents/relatives F yes Saudi Arabia - - - - - EE see paper; ..., severe early infantile encephalopathy, progressive microcephaly, axial hypotonia, appendicular hypertonia, refractory epilepsy 1 2 Johan den Dunnen
00301744 17-3196 PubMed: Maddirevula 20198 - - - - - - - - - ? global developmental delay, progressive microcephaly 1 1 Johan den Dunnen
00301745 17-3892 PubMed: Maddirevula 20198 - - - - - - - - - ? global developmental delay, progressive microcephaly 1 1 Johan den Dunnen
00361535 12DG1577 PubMed: Anazi 2017 familial F yes Saudi Arabia - - - - - ID not syndromic; Neurodegeneration 1 1 Johan den Dunnen
00426164 10DF14100 PubMed: Al-Kasbi 2022 patient, other affecteds in family M - Oman - - - - - ID - 1 1 Johan den Dunnen
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