De novo mutations in KIF1A cause progressive encephalopathy and brain atrophy

OBJECTIVE: To determine the cause and course of a novel syndrome with progressive encephalopathy and brain atrophy in children. METHODS: Clinical whole-exome sequencing was performed for global developmental delay and intellectual disability; some patients also had spastic paraparesis and evidence o...

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Detalles Bibliográficos
Autores principales: Esmaeeli Nieh, Sahar, Madou, Maura R Z, Sirajuddin, Minhajuddin, Fregeau, Brieana, McKnight, Dianalee, Lexa, Katrina, Strober, Jonathan, Spaeth, Christine, Hallinan, Barbara E, Smaoui, Nizar, Pappas, John G, Burrow, Thomas A, McDonald, Marie T, Latibashvili, Mariam, Leshinsky-Silver, Esther, Lev, Dorit, Blumkin, Luba, Vale, Ronald D, Barkovich, Anthony James, Sherr, Elliott H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2015
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4479523/
https://www.ncbi.nlm.nih.gov/pubmed/26125038
http://dx.doi.org/10.1002/acn3.198

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4479523/
https://www.ncbi.nlm.nih.gov/pubmed/26125038
http://dx.doi.org/10.1002/acn3.198

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