A novel LITAF/SIMPLE mutation within a family with a demyelinating form of Charcot-Marie-Tooth disease

Medicine and Dentistry

• Lysosome 100%
• Membrane Protein 100%
• Endosome 100%
• DeJerine-Sottas Disease 80%
• Family 60%
• Diseases 40%
• Missense Mutation 40%
• Nerve Block 40%
• Diagnosis 20%
• Lower Limb 20%
• Genetic Analysis 20%
• Onset Age 20%
• Pedigree 20%
• Nerve Conduction Study 20%
• Demyelination 20%
• Analysis 20%
• Patient 20%

Biochemistry, Genetics and Molecular Biology

• Integral Membrane Protein 100%
• Lysosome 100%
• Mutation 40%
• Missense Mutation 40%
• Nerve Block 40%
• Genetics 40%
• LITAF 40%
• Pedigree 20%
• Nerve Conduction Study 20%
• Age 20%
• Flow 20%

Neuroscience

• Charcot-Marie-Tooth Disease 80%
• Missense Mutation 40%
• Peripheral Nervous System 40%
• Nerve Conduction Study 20%