Exome sequencing reveals a homozygous frameshift variant in CAPN3 in a Tunisian patient with a neuromuscular disorder

JOURNAL ARTICLE published 27 September 2022 in Annals of Molecular and Genetic Medicine

Authors: Foddha Hajer | Seo Go Hun | Lee Hane | Zemzem Firas | Naouar Ines | Boughammoura Amel | Gribaa Moez | Khelil Amel Haj