All individuals with variants in gene ISCA2

5 entries on 1 page. Showing entries 1 - 5.
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00034035 - PubMed: Al-Hassnan 2015, Journal: Al-Hassnan 2015 5 families, 8 affecteds (5F, 3M), unaffected heterozygous carrier parents/sibs - - Saudi Arabia - - - - - ? see paper; infantile-onset neurodegenerative manifestations, severe leukodystrophy, ... 1 8 Johan den Dunnen
00080929 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - MMDS4 Multiple m dysfunctions syndrome type 4 (OMIM:616370) 1 1 Daniel Trujillano
00225702 25558065-Fam14DG0152 PubMed: Alazami 2015, Journal: Alazami 2015 4-generation family, 6 affected (3F, 3M), unaffected heterozygous carrier parents/relatives F;M yes Saudi Arabia - - - - - ? see paper; …, neurodegeneration with marked white matter changes with high lactate peak in the brain, consistent with mitochondrial encephalopathy 1 6 Johan den Dunnen
00361558 14DG0152 PubMed: Anazi 2017 familial F yes Saudi Arabia - - - - - ID not syndromic; Neurodegeneration, marked white matter changes with high lactate peak in the brain 1 1 Johan den Dunnen
00415259 14 PubMed: Alfares 2018 - M - - - - - - - retinal disease OMIM: 616370; seizures, choking episodes 1 1 LOVD
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