Sign Up to like & get
recommendations!
1
Published in 2022 at "Epilepsy Research"
DOI: 10.1016/j.eplepsyres.2022.106923
Abstract: INTRODUCTION Disorders associated with mutations in the Tre2/Bub2/Cdc16 (TBC)1 domain family member 24 gene (TBC1D24) present a wide range of phenotypes, ranging from mild to fatal seizure diseases, non-syndromic deafness, and complex syndromes such as…
read more here.
Keywords:
tbc1d24 related;
myoclonic epilepsy;
familial infantile;
homozygous tbc1d24 ... See more keywords