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Publications by Inger Nennesmo
A Pan-European Study of theC9orf72Repeat Associated With FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats
Human Mutation
Genetics
Early Activating Somatic PIK3CA Mutations Promote Ectopic Muscle Development and Upper Limb Overgrowth
Clinical Genetics
Genetics
Respiratory Chain Complex III Deficiency Due to Mutated BCS1L: A Novel Phenotype With Encephalomyopathy, Partially Phenocopied in a Bcs1l Mutant Mouse Model
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology