Armirola-Ricaurte, C. Et Al. 2022. Screening of SORD mutations in a CMT cohort expands the clinical spectrum of SORD-related neuropathy. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1 , 309-310.

Armirola-Ricaurte, C., de Vriendt, E., Candayan, A., Asenov, O., Parman, Y., Chamova, T., ... Tournev, I.(2022). Screening of SORD mutations in a CMT cohort expands the clinical spectrum of SORD-related neuropathy. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1, 309-310.

Armirola-Ricaurte, Camila Et Al. "Screening of SORD mutations in a CMT cohort expands the clinical spectrum of SORD-related neuropathy," EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1, 309-310, 2022

Armirola-Ricaurte, Camila Et Al. "Screening of SORD mutations in a CMT cohort expands the clinical spectrum of SORD-related neuropathy." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1, pp.309-310, 2022

Armirola-Ricaurte, C. Et Al. (2022) . "Screening of SORD mutations in a CMT cohort expands the clinical spectrum of SORD-related neuropathy." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1, pp.309-310.

@article{article, author={Camila Armirola-Ricaurte Et Al. }, title={Screening of SORD mutations in a CMT cohort expands the clinical spectrum of SORD-related neuropathy}, journal={EUROPEAN JOURNAL OF HUMAN GENETICS}, year=2022, pages={309-310} }