Résultats de la recherche

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TMEM240 mutations cause spinocerebellar ataxia 21 with mental retardation and severe cognitive impairment
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1

Islandora displays