Last Updated: 09/26/2026
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Found 4 publications
Novel homozygous mutation in the FBXL4 gene is associated with mitochondria DNA depletion syndrome-13.
Journal: Journal of the neurological sciences
Published: October 31, 2019
Bumbling, Stumbling, Fumbling: Weakness, Steppage Gait, and Facial Droop in a 3-Year-Old Male.
Journal: Global pediatric health
Published: May 15, 2019
Sleep Disorders in Childhood Neurological Diseases.
Journal: Children (Basel, Switzerland)
Published: May 24, 2017
Diagnosis and management of childhood epilepsy.
Journal: Current problems in pediatric and adolescent health care
Published: December 01, 2014
Showing 1-4 of 4
Last Updated: 09/26/2026