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You searched for: Author/Creator Dimberg, Elliot L.

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12. Whole Exome Sequencing Leading to the Diagnosis of Dysferlinopathy with a Novel Missense Mutation (c.959G>C). (19th April 2016)

13. Whole exome sequencing of a patient with suspected mitochondrial myopathy reveals novel compound heterozygous variants in RYR1. Issue 3 (30th March 2017)