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Your search keyword '"Strømme, Petter"' showing total 9 results

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9 results on '"Strømme, Petter"'

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1. Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals

2. DNA methylation episignature in Gabriele-de Vries syndrome

4. Clinical and molecular characteristics in three families with biallelic mutations in IGHMBP2

5. A novel mutation in FBXL4 in a Norwegian child with encephalomyopathic mitochondrial DNA depletion syndrome 13

8. SLC9A6 Mutations Cause X-Linked Mental Retardation, Microcephaly, Epilepsy, and Ataxia, a Phenotype Mimicking Angelman Syndrome

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