AA
Asmaa F. Abdel‐Aleem

Publications (2)

ADAT3-related neurodevelopmental disorder in 24 new patients with a high frequency of the p.Val144Met and a new founder variant
Article scientifique · 2025
A novel founder variant in BEST1 gene causing autosomal recessive bestrophinopathy
Article scientifique · 2025

Domaines principaux

Sciences de la vie et biotechnologies2

Statistiques

Consultations3
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