Optimized testing strategy for the diagnosis of GAA-FGF14 ataxia/spinocerebellar ataxia 27BCéline Bonnet, M. Renaud, Frédéric Weber et al.|Scientific Reports|2023Cited by 72
Frequency and phenotypic spectrum of spinocerebellar ataxia <scp>27B</scp> and other genetic ataxias in a Spanish cohort of late‐onset cerebellar ataxiaPablo Iruzubieta, Javier Ruiz‐Martínez, David Pellerin et al.|European Journal of Neurology|2023Cited by 39
Frequency of GAA- <i>FGF14</i> Ataxia in a Large Cohort of Brazilian Patients With Unsolved Adult-Onset Cerebellar AtaxiaLuiz Eduardo Novis, Hélio Afonso Ghizoni Teive, Rodrigo Siqueira Soares Frezatti et al.|Neurology Genetics|2023Cited by 36
The <i>FGF14</i> <scp>GAA</scp> repeat expansion in Greek patients with late‐onset cerebellar ataxia and an overview of the <scp>SCA27B</scp> phenotype across populationsChrisoula Kartanou, Georgios Koutsis, Alexandros Mitrousias et al.|Clinical Genetics|2024Cited by 28
<scp>Non‐GAA</scp> Repeat Expansions in <scp><i>FGF14</i></scp> Are Likely Not Pathogenic—Reply to: “<i>Shaking Up Ataxia</i>: <scp><i>FGF14</i></scp> and <scp><i>RFC1</i></scp> Repeat Expansions in Affected and Unaffected Members of a Chilean Family”David Pellerin, Henry Houlden, Pablo Iruzubieta et al.|Movement Disorders|2023Cited by 24