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Last Updated: 10/31/2025
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Found 17 publications
CMT4J, parkinsonism and a new FIG4 mutation.
Journal: Parkinsonism & related disorders
Published: May 16, 2020
Clinical and radiological characterization of novel FIG4-related combined system disease with neuropathy.
Journal: Clinical genetics
Published: February 05, 2020
FIG4 mutations leading to parkinsonism and a phenotypical continuum between CMT4J and Yunis Varón syndrome.
Journal: Parkinsonism & related disorders
Published: October 10, 2019
Homozygous variant, p.(Arg643Trp) in VAC14 causes striatonigral degeneration: report of a novel variant and review of VAC14-related disorders.
Journal: Journal of human genetics
Published: July 27, 2019
Yunis-Varon Syndrome.
Journal: Journal of Ayub Medical College, Abbottabad : JAMC
Published: May 17, 2019
Protective role of the lipid phosphatase Fig4 in the adult nervous system.
Journal: Human molecular genetics
Published: March 16, 2018
Yunis-Varón syndrome caused by biallelic VAC14 mutations.
Journal: European journal of human genetics : EJHG
Published: March 01, 2017
Rescue of neurodegeneration in the Fig4 null mouse by a catalytically inactive FIG4 transgene.
Journal: Human molecular genetics
Published: September 03, 2015
Yunis-Varón syndrome: the first report of two Iranian cases.
Journal: Acta medica Iranica
Published: February 19, 2014
Novel FIG4 mutations in Yunis-Varon syndrome.
Journal: Journal of human genetics
Published: June 27, 2013
Yunis-Varón syndrome is caused by mutations in FIG4, encoding a phosphoinositide phosphatase.
Journal: American journal of human genetics
Published: January 29, 2013
Last Updated: 10/31/2025