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Author response for "Novel pathogenic <scp> <i>EIF2S3</i> </scp> missense variants causing clinically variable <scp>MEHMO</scp> syndrome with impaired <scp>eIF2γ</scp> translational function, and literature review"
Identifier:nobleid.org/w1/20260515/DAFEC5CF
Type:Journal Article
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