Cargando…
Novel HSPB1 mutation causes both motor neuronopathy and distal myopathy
OBJECTIVE: To identify the cause of isolated distal weakness in a family with both neuropathic and myopathic features on EMG and muscle histology. METHODS: Case study with exome sequencing in 2 affected individuals, bioinformatic prioritization of genetic variants, and segregation analysis of the li...
Autores principales: | Lewis-Smith, D.J., Duff, J., Pyle, A., Griffin, H., Polvikoski, T., Birchall, D., Horvath, R., Chinnery, P.F. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5089436/ https://www.ncbi.nlm.nih.gov/pubmed/27830184 http://dx.doi.org/10.1212/NXG.0000000000000110 |
Ejemplares similares
-
Homozygous mutation in HSPB1 causing distal vacuolar myopathy and motor neuropathy
por: Bugiardini, Enrico, et al.
Publicado: (2017) -
A knock-in/knock-out mouse model of HSPB8-associated distal hereditary motor neuropathy and myopathy reveals toxic gain-of-function of mutant Hspb8
por: Bouhy, Delphine, et al.
Publicado: (2017) -
Reply: Hereditary myopathy with early respiratory failure is caused by mutations in the titin FN3 119 domain
por: Pfeffer, Gerald, et al.
Publicado: (2014) -
The p.Ser107Leu in BICD2 is a mutation ‘hot spot’ causing distal spinal muscular atrophy
por: Bansagi, Boglarka, et al.
Publicado: (2015) -
Distal hereditary motor neuronopathy of the Jerash type is caused by a novel SIGMAR1 c.500A>T missense mutation
por: Ververis, Antonis, et al.
Publicado: (2020)