4 results on '"Strømme, Petter"'
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2. Novel Loss of Function Variants in CENPF including a Large Intragenic Deletion in Patients with Strømme Syndrome
3. Novel PIGT Variant in Two Brothers: Expansion of the Multiple Congenital Anomalies-Hypotonia Seizures Syndrome 3 Phenotype
4. Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
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