Tremor Ataxia With Central Hypomyelation Phenotype Related to a Recurrent POLR3A Mutation in Six Unrelated Tunisian Families.
Kraoua I, Jamoussi M, Drissi C, Kraoua L, Drunat S, Benrhouma H, Ben Younes T, Nagi S, Abdelhak S, Boespflug Tanguy O, Youssef-Turki IB, Trabelsi M, Dorboz I.
Kraoua I, et al. Among authors: ben younes t.
Mol Genet Genomic Med. 2024 Oct;12(10):e70007. doi: 10.1002/mgg3.70007.
Mol Genet Genomic Med. 2024.
PMID: 39436788
Free PMC article.