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Fingerprint Dive into the research topics where Emanuele Bellacchio is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

Medicine & Life Sciences

Mutation
Genes
Phenotype
Missense Mutation
Ataxia
Myotonia Congenita
Proteins
Cofilin 2
Muscles
Muscular Diseases
Exome
Anhidrotic Ectodermal Dysplasia 3
Intellectual Disability
Mitochondrial Diseases
Cerebellar Ataxia
Dynamin I
Brain Diseases
Nuclear Pore Complex Proteins
Apoptosis Inducing Factor
Regulator Genes
Italy
Noonan Syndrome
Oncogene Proteins
Computer Simulation
Marfan Syndrome
Motor Neuron Disease
Human papillomavirus 16
Homeostasis
Iris
Atrophy
Brain
Spinocerebellar Degenerations
Addison Disease
Anhidrotic Ectodermal Dysplasia 1
Tubulin
Hypobetalipoproteinemia, Familial, Apolipoprotein B
Myosins
Molecular Biology
Biopsy
Neurons
Exons
Cell Survival
Deafness
Mitochondria
Parkinson Disease
Charcot-Marie-Tooth Disease
Autoimmune Polyendocrinopathies
Microtubules
Sensorineural Hearing Loss
Familial Partial Lipodystrophy