Genetic testing for monogenic forms of motor neuron disease/amyotrophic lateral sclerosis in unaffected family members
Motor neuron disease (MND), also referred to as amyotrophic lateral sclerosis (ALS), is a monogenic disease in a minority of cases, with autosomal dominant inheritance. Increasing numbers of people with MND are requesting genetic testing, and indeed receiving a genetic diagnosis. Consequently, reque...
Huvudupphovsmän: | Howard, J, Chaouch, A, Douglas, AGL, MacLeod, R, Roggenbuck, J, McNeill, A |
---|---|
Materialtyp: | Journal article |
Språk: | English |
Publicerad: |
Springer Nature [academic journals on nature.com]
2024
|
Liknande verk
Liknande verk
-
Neuronal Circuit Dysfunction in Amyotrophic Lateral Sclerosis
av: Andrea Salzinger, et al.
Publicerad: (2024-05-01) -
Assessment of the upper motor neuron in amyotrophic lateral sclerosis
av: Huynh, W, et al.
Publicerad: (2016) -
Searching Far and Genome-Wide: The Relevance of Association Studies in Amyotrophic Lateral Sclerosis
av: Kelly A. Rich, et al.
Publicerad: (2021-01-01) -
Motor neuron replacement therapy for amyotrophic lateral sclerosis
av: Bochao Liu, et al.
Publicerad: (2022-01-01) -
Telehealth-based exercise in amyotrophic lateral sclerosis
av: Virginia Kudritzki, et al.
Publicerad: (2023-07-01)