Cita APA

Exome sequencing reveals a homozygous frameshift variant in CAPN3 in a Tunisian patient with a neuromuscular disorder. (2022). Exome sequencing reveals a homozygous frameshift variant in CAPN3 in a Tunisian patient with a neuromuscular disorder. Annals of Molecular and Genetic Medicine - Peertechz Publications. https://doi.org/10.17352/amgm.000010

Citación estilo Chicago

Exome sequencing reveals a homozygous frameshift variant in CAPN3 in a Tunisian patient with a neuromuscular disorder. Exome Sequencing Reveals a Homozygous Frameshift Variant in CAPN3 in a Tunisian Patient with a Neuromuscular Disorder. Annals of Molecular and Genetic Medicine - Peertechz Publications, 2022. https://doi.org/10.17352/amgm.000010.

Cita MLA

Exome sequencing reveals a homozygous frameshift variant in CAPN3 in a Tunisian patient with a neuromuscular disorder. Exome Sequencing Reveals a Homozygous Frameshift Variant in CAPN3 in a Tunisian Patient with a Neuromuscular Disorder. Annals of Molecular and Genetic Medicine - Peertechz Publications, 2022. https://doi.org/10.17352/amgm.000010.