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2022
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2017
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Association of Pathway Mutations With Survival in Taiwanese Breast Cancers.
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S-EPMC9354680
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biostudies-literature
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A Recurrent De Novo Variant in NACC1 Causes a Syndrome Characterized by Infantile Epilepsy, Cataracts, and Profound Developmental Delay.
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S-EPMC5294886
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biostudies-literature
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