Drögemöller Lab
Drögemöller Lab
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Jessica Lee
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Secondary biogenic amine deficiencies: Genetic etiology, therapeutic interventions and clinical effects
Atypical cerebral palsy: genomics analysis enables precision medicine
Germline de novo mutations in ATP1A1 cause renal hypomagnesemia, refractory seizures, and intellectual disability
Further validation of the SIGMAR1 c.151+1G>T mutation as cause of distal hereditary motor neuropathy
Exome sequencing and the management of neurometabolic disorders
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