Drögemöller Lab
Drögemöller Lab
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Ingrid Blydt-Hansen
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Secondary biogenic amine deficiencies: Genetic etiology, therapeutic interventions and clinical effects
Atypical cerebral palsy: genomics analysis enables precision medicine
Gain-of-function KCNJ6 mutation in a severe hyperkinetic movement disorder phenotype
A de novo mosaic mutation in SPAST with two novel alternative alleles and chromosomal copy number variant in a boy with spastic paraplegia and autism spectrum disorder
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