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Heterozygous Mutation in the KCNMA1 Gene with “Loss of Function” Phenotype in a Patient with Generalized Epilepsy
Heterozygous Mutation in the KCNMA1 Gene with “Loss of Function” Phenotype in a Patient with Generalized Epilepsy
2015
S. Poschmann
M. Baethmann
S. Biskup
Steffen Leiz
Keywords:
KCNMA1 Gene
Loss function
Diabetes mellitus
Phenotype
Genetics
Generalized epilepsy
Medicine
Mutation
Bioinformatics
heterozygous mutation
Correction
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