{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Ashrafi MR"],"funding":["National Institute for Medical Research Development"],"pagination":["1125-1132"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC8914440"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["72(5)"],"pubmed_abstract":["Introduction
Coenzyme Q10 deficiency can be due to mutations in Coenzyme Q10-biosynthesis genes (primary) or genes unrelated to biosynthesis (secondary). Primary Coenzyme Q10 deficiency-4 (COQ10D4), also known as autosomal recessive spinocerebellar ataxia-9 (SCAR9), is an autosomal recessive disorder caused by mutations in the ADCK3 gene. This disorder is characterized by several clinical manifestations such as severe infantile multisystemic illness, encephalomyopathy, isolated myopathy, cerebellar ataxia, or nephrotic syndrome.Methods
In this study, whole-exome sequencing was performed in order to identify disease-causing variants in an affected girl with developmental regression and Epilepsia Partialis Continua (EPC). Next, Sanger sequencing method was used to confirm the"],"journal":["Journal of molecular neuroscience : MN"],"pubmed_title":["Epilepsia Partialis Continua a Clinical Feature of a Missense Variant in the ADCK3 Gene and Poor Response to Therapy."],"pmcid":["PMC8914440"],"funding_grant_id":["971846"],"pubmed_authors":["Mahdieh N","Rezaei Z","Tavasoli AR","Mohammadi P","Ghabeli H","Badv RS","Heidari M","Ashrafi MR","Haghighi R","Pourbakhtyaran E"],"additional_accession":[]},"is_claimable":false,"name":"Epilepsia Partialis Continua a Clinical Feature of a Missense Variant in the ADCK3 Gene and Poor Response to Therapy.","description":"Introduction
Coenzyme Q10 deficiency can be due to mutations in Coenzyme Q10-biosynthesis genes (primary) or genes unrelated to biosynthesis (secondary). Primary Coenzyme Q10 deficiency-4 (COQ10D4), also known as autosomal recessive spinocerebellar ataxia-9 (SCAR9), is an autosomal recessive disorder caused by mutations in the ADCK3 gene. This disorder is characterized by several clinical manifestations such as severe infantile multisystemic illness, encephalomyopathy, isolated myopathy, cerebellar ataxia, or nephrotic syndrome.Methods
In this study, whole-exome sequencing was performed in order to identify disease-causing variants in an affected girl with developmental regression and Epilepsia Partialis Continua (EPC). Next, Sanger sequencing method was used to confirm the","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 May","modification":"2025-05-18T12:33:54.079Z","creation":"2025-04-06T12:01:40.255Z"},"accession":"S-EPMC8914440","cross_references":{"pubmed":["35275351"],"doi":["10.1007/s12031-022-01993-0"]}}