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CHCHD10 mutations and motor neuron disease: the distribution in Finnish patients.
https://arctichealth.org/en/permalink/ahliterature295775
Source
J Neurol Neurosurg Psychiatry. 2017 03; 88(3):272-277
Publication Type
Journal Article
Date
03-2017
More detail
Author
Sini Penttilä
Manu Jokela
Anna Maija Saukkonen
Jari Toivanen
Johanna Palmio
Janne Lähdesmäki
Satu Sandell
Mariia Shcherbii
Mari Auranen
Emil Ylikallio
Henna Tyynismaa
Bjarne Udd
Author Affiliation
Neuromuscular Research Center, Tampere University and University Hospital, Tampere, Finland.
Source
J Neurol Neurosurg Psychiatry. 2017 03; 88(3):272-277
Date
03-2017
Language
English
Publication Type
Journal Article
Keywords
Adult
Aged
Aged, 80 and over
Amyotrophic Lateral Sclerosis - genetics - physiopathology
Biopsy
Charcot-Marie-Tooth Disease - genetics
Cohort Studies
Electromyography
European Continental Ancestry Group - genetics
Female
Finland
Humans
Male
Middle Aged
Mitochondrial Myopathies - genetics - physiopathology
Mitochondrial Proteins - genetics
Motor Neuron Disease - genetics - physiopathology
Muscle, Skeletal - pathology - physiopathology
Muscular Atrophy, Spinal - genetics - pathology - physiopathology
Mutation
Phenotype
Spastic Paraplegia, Hereditary - genetics - physiopathology
PubMed ID
27810918
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