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Sfari Gene

Shobhit Saxena

Abstract


Recent studies have demonstrated that segmental dosage variants, rare de novo nucleotide sequence variations and inherited rare common sequence variants all play vital role in the etiology of autism. The major rakishness with the genes and autism majorly Sfari genes are reviewed in this paper.

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DOI: https://doi.org/10.37628/ijcbb.v3i1.172

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