A de novo dominant mutation in KIF1A associated with axonal neuropathy, spasticity and autism spectrum disorder

Mutations in the kinesin family member 1A (KIF1A) gene have been associated with a wide range of phenotypes including recessive mutations causing hereditary sensory neuropathy and hereditary spastic paraplegia and de novo dominant mutations causing a more complex neurological disorder affecting both...

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Detalles Bibliográficos
Autores principales: Tomaselli, Pedro J., Rossor, Alexander M., Horga, Alejandro, Laura, Matilde, Blake, Julian C., Houlden, Henry, Reilly, Mary M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Periodicals, Inc. 2017
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5763335/
https://www.ncbi.nlm.nih.gov/pubmed/28834584
http://dx.doi.org/10.1111/jns.12235

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5763335/
https://www.ncbi.nlm.nih.gov/pubmed/28834584
http://dx.doi.org/10.1111/jns.12235

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