Medicine and Dentistry
Disease
100%
Neurofilament
100%
Autosomal Dominant Inheritance
50%
DeJerine-Sottas Disease
50%
Autosomal Recessive Inheritance
50%
Missense Mutation
50%
Myelin Protein
50%
Kinesin
50%
Multifocal Motor Neuropathy
50%
Sensory Neuropathy
50%
Connexin 32
50%
Keyphrases
Neurofilament Light (NF-L)
100%
CMT2
100%
Autosomal Dominant
16%
Motor Neuropathy
16%
Autosomal Recessive
16%
Novel mutation
16%
Charcot-Marie-Tooth Disease
16%
Connexin 32
16%
Missense mutation
16%
Most Common Form
16%
CMT2C
16%
1q21.1
16%
CMT2B
16%
CMT2E
16%
CMT2A
16%
Co-segregation
16%
CMT2F
16%
CMT2D
16%
Two-locus Model
16%
Sensory Neuropathy
16%
Myelin Protein Zero
16%
Genetic Localization
16%
Kinesin
16%
Neuroscience
Neurofilament
100%
Missense Mutation
50%
Charcot-Marie-Tooth Disease
50%
Kinesin
50%
Myelin Protein
50%
Connexin 32
50%
Neuropathy
50%
Biochemistry, Genetics and Molecular Biology
Neurofilament Light
100%
Gap Junction Protein
33%