Manar Salameh
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Neurogenetics
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Clinical genetics
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Sep 30, 2026
A Homozygous Frameshift Variant in KHDC4 Is Associated With a Syndromic Inherited Retinal Disease in Humans.
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Dror Sharon
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Asodu Sandeep Sarma
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Prakadeeswari Gopalakrishnan
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Dror Sharon
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