Mutation spectrum of Joubert syndrome and related disorders among Arabs

Joubert syndrome (JS) is a rare autosomal recessive (AR), neurological condition characterized by dysgenesis of the cerebellar vermis with the radiological hallmark of molar tooth sign, oculomotor apraxia, recurrent hyperventilation and intellectual disability. Most cases display a broad spectrum of...

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Detalles Bibliográficos
Autores principales: Ben-Salem, Salma, Al-Shamsi, Aisha M, Gleeson, Joseph G, Ali, Bassam R, Al-Gazali, Lihadh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4785524/
https://www.ncbi.nlm.nih.gov/pubmed/27081510
http://dx.doi.org/10.1038/hgv.2014.20

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4785524/
https://www.ncbi.nlm.nih.gov/pubmed/27081510
http://dx.doi.org/10.1038/hgv.2014.20

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