All individuals with variants in gene CYP2U1

10 entries on 1 page. Showing entries 1 - 10.
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00080879 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - SPG56 Spastic paraplegia 56, autosomal recessive (OMIM:615030) 1 1 Daniel Trujillano
00131878 Case 1 Durand et al., in revision - M yes Turkey - >12y - - - SPG56 - 1 1 Isabelle Coupry
00131884 Case 2 Durand et al., in revision - M no Italy - 08y - - - SPG56 - 1 1 Isabelle Coupry
00295759 - - - M - - - - - - - ? Spastic paraparesis (HP:0002313); Abnormal muscle tone (HP:0003808) 1 1 Andreas Laner
00361515 10DG0886 PubMed: Anazi 2017 familial M yes Saudi Arabia - - - - - ID not syndromic; intellectual disability with spastic paraplegia 1 1 Johan den Dunnen
00408395 - - - - - - - - - - - maculopathy - 1 1 Oscar F Chacon-Camacho
00415252 7 PubMed: Alfares 2018 - M - - - - - - - retinal disease OMIM: 615030; spastic paraplegia 1 1 LOVD
00448056 274491 - - M likely ? (unknown) - - - - - SPG56 Abnormality of movement, Spastic paraparesis, Unsteady gait 1 1 Andreas Laner
00454720 NGSP65 PubMed: Legati 2016 2-generation family, 1 affected, unaffected heterozygous carrier parents M yes - - - - - - mitochondrial psycomotor regression, diabetes, intellectual disability, leukoencephalopathy 1 1 Daniele Ghezzi
00466506 patient PubMed: Saneto 2022, Journal: Saneto 2022 - M - United States - - - - - SPG see paper; ... 2 1 Johan den Dunnen
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