Family-base rare variant association analysis in Saudi Arabian hydrocephalus subjects using whole exome sequencing.
Ammar A, Bubshait DK, Al Ojan A, Alshari SA, Cyrus C, Alanazi R, Al Ghamdi MA, Keating BJ, Al-Anazi A, Al Qahtani NH, Al-Ali AK.
Ammar A, et al. Among authors: al anazi a, al ghamdi ma, al qahtani nh, al ali ak, al ojan a.
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J Neurosurg Sci. 2024.
PMID: 37158713
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