Anshika Srivastava

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0CO-AUTHORS
Neurogenetics
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Publications (1)

|Jun 20, 2023
A novel biallelic frameshift variant in C2orf69 causing developmental regression, seizures, microcephaly, autistic features, and hypertonia.

Elizabeth A Werren, Varunvenkat M Srinivasan, Vykuntaraju K Gowda

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