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Ataxie Télangiectasie
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    missing heritability

    • Case Report: Biallelic Loss of Function ATM due to Pathogenic Synonymous and Novel Deep Intronic Variant c.1803-270T > G Identified by Genome Sequencing in a Child With Ataxia-Telangiectasia

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    Ataxie Télangiectasie
      • Home
      • Qu’est-ce que l’A-T ?
      • Nouvelles
      • admin@ataxiatelangiectasia.es