Progressive myoclonic ataxia and developmental/epileptic encephalopathy associated with a novel homozygous mutation in TCN2 gene
Oshi, Mohammed Ahmed Mohammed, Alfaifi, Jaber, Alqahtani, Youssef Ali M., Aljabri, Mohammed Fahad, Kamal, Naglaa M., Althopaity, Jwaher, Althobaiti, Khalid A., Almalki, Abdullah M., Abosabie, Salma A. S., Abosabie, Sara A., Sherbiny, Hanan Sakr, Almanjoomi, Saif K., Abdallah, Enas A. A.
Published in Molecular genetics & genomic medicine (01.01.2024)
Published in Molecular genetics & genomic medicine (01.01.2024)
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Journal Article
Progressive myoclonic ataxia and developmental/epileptic encephalopathy associated with a novel homozygous mutation in TCN 2 gene
Oshi, Mohammed Ahmed Mohammed, Alfaifi, Jaber, Alqahtani, Youssef Ali M., Aljabri, Mohammed Fahad, Kamal, Naglaa M., Althopaity, Jwaher, Althobaiti, Khalid A., Almalki, Abdullah M., Abosabie, Salma A. S., Abosabie, Sara A., Sherbiny, Hanan Sakr, Almanjoomi, Saif K., Abdallah, Enas A. A.
Published in Molecular genetics & genomic medicine (01.01.2024)
Published in Molecular genetics & genomic medicine (01.01.2024)
Get full text
Journal Article