Exome sequencing reveals a homozygous frameshift variant in CAPN3 in a Tunisian patient with a neuromuscular disorder
Crossref DOI link: https://doi.org/10.17352/amgm.000010
Published Online: 2022-09-27
Update policy: https://doi.org/10.17352/crossmark-policy
Hajer, Foddha
Go Hun, Seo
Hane, Lee
Firas, Zemzem
Ines, Naouar
Amel, Boughammoura
Moez, Gribaa
Amel Haj, Khelil https://orcid.org/0000-0001-5666-2116
