Associated Papers
A homozygous ARMC3 splicing variant causes asthenozoospermia and flagellar disorganization in a consanguineous family.
Rahim F et al.
Clinical Genetics, 2024
Undiagnosed Rare Genetic Disorders: Importance of Functional Characterization of Variants.
Umair M et al.
Genes, 2023
The Expansion of the Spectrum in Stuttering Disorders to a Novel ARMC Gene Family (ARMC3).
Rehman AU et al.
Genes, 2022
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