Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxiaAndrea Cortese, Henry Houlden, Roberto Simone et al.|Nature Genetics|2019Cited by 592
<i>PDXK</i> mutations cause polyneuropathy responsive to pyridoxal 5′‐phosphate supplementationViorica Chelban, Henry Houlden, Yo‐Tsen Liu et al.|Annals of Neurology|2019Cited by 75
Mutations in NKX6-2 Cause Progressive Spastic Ataxia and HypomyelinationViorica Chelban, Henry Houlden, Nisha Patel et al.|The American Journal of Human Genetics|2017Cited by 51
Author Correction: Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxiaAndrea Cortese, Henry Houlden, Roberto Simone et al.|Nature Genetics|2019Cited by 14
15.09 Inherited peripheral neuropathies: analysis of PDXK gene identifies a new treatable disorderViorica Chelban, Henry Houlden, Matthew P. Wilson et al.|Journal of Neurology Neurosurgery & Psychiatry|2019Cited by 0