AKU eCommons
Ehtisham Ul, Haq Makhdoom, S. S. Waseem et al.
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Open access
Aug 2026
Homozygous missense variants in CACNB4 underlie autosomal recessive epilepsy in two unrelated Pakistani consanguineous families.
This is the second report of autosomal recessive epilepsy associated with biallelic CACNB4 variants and genetic investigations play a crucial role in identifying mutation hotspots, facilitating more accurate diagnoses and enhancing the design of diagnostic panels for early detection.
Anwar Ullah, Fazl Ullah, Irfan Ullah et al.
· Seizure · 0 citations