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OTUD7A inhibits Syndrome. 1 / 1

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"Possibly, a heterozygous deletion of OTUD7A leads to a disruption of the ubiquitination pathway and contributes to the phenotypic overlap between patients with AS and patients with the 15q13.3 deletio[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"

20382277

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IndraLab

Statements

OTUD7A inhibits Syndrome. 1 / 1

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