UFM1 founder mutation in the Roma population causes recessive variant of H-ABC

OBJECTIVE: To identify the gene defect in patients with hypomyelination with atrophy of the basal ganglia and cerebellum (H-ABC) who are negative for TUBB4A mutations. METHODS: We performed homozygosity mapping and whole exome sequencing (WES) to detect the disease-causing variant. We used a Taqman...

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Detalles Bibliográficos
Autores principales: Hamilton, Eline M.C., Bertini, Enrico, Kalaydjieva, Luba, Morar, Bharti, Dojčáková, Dana, Liu, Judy, Vanderver, Adeline, Curiel, Julian, Persoon, Claudia M., Diodato, Daria, Pinelli, Lorenzo, van der Meij, Nathalie L., Plecko, Barbara, Blaser, Susan, Wolf, Nicole I., Waisfisz, Quinten, Abbink, Truus E.M., van der Knaap, Marjo S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5664304/
https://www.ncbi.nlm.nih.gov/pubmed/28931644
http://dx.doi.org/10.1212/WNL.0000000000004578

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5664304/
https://www.ncbi.nlm.nih.gov/pubmed/28931644
http://dx.doi.org/10.1212/WNL.0000000000004578

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