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You searched for: Author/Creator Khan, Nasaim

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1. Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1. (16th January 2015)

4. Role of reverse phenotyping in interpretation of next generation sequencing data and a review of INPP5E related disorders. (March 2016)