All individuals with variants in gene NSUN3

3 entries on 1 page. Showing entries 1 - 3.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00390470 A016105 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - (United Kingdom (Great Britain)) - - - - - ? - 1 1 LOVD
00431244 patient;R18626 PubMed: Van Haute 2016, PubMed: Yepez 2022 2-generation family, 1 affected, unaffected heterozygous carrier parents M - Germany - - - - - ? 3m-combined developmental disability, microcephaly, failure to thrive, recurrent increased lactate levels in plasma, muscular weakness, proximal accentuated, external ophthalmoplegia, convergence nystagmus, combined OXPHOS deficiency skeletal muscle 2 1 Johan den Dunnen
00436494 FamPatII3 PubMed: Paramasivam 2020 2-generation family, 1 affected (deceased older sister), unaffected heterozygous parents M yes India - - - - - ? see paper; ..., early-onset mitochondrial encephalomyopathy; 4m-lactic acidosis, global developmental delay, hypotonia, muscle weakness, seizures 2 1 Johan den Dunnen
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.