Associated Papers
Genome Sequencing Identifies 13 Novel Candidate Risk Genes for Autism Spectrum Disorder in a Qatari Cohort.
Ben-Mahmoud A et al.
International Journal of Molecular Sciences, 2024
Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss.
Ramzan K et al.
Genes, 2020
33316915 (PubMed )
Supplement: genes-11-01474-s001.pdf
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