Spectrum of PEX1 and PEX6 variants in Heimler syndrome

Heimler syndrome (HS) consists of recessively inherited sensorineural hearing loss, amelogenesis imperfecta (AI) and nail abnormalities, with or without visual defects. Recently HS was shown to result from hypomorphic mutations in PEX1 or PEX6, both previously implicated in Zellweger Syndrome Spectr...

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Detalles Bibliográficos
Autores principales: Smith, Claire E L, Poulter, James A, Levin, Alex V, Capasso, Jenina E, Price, Susan, Ben-Yosef, Tamar, Sharony, Reuven, Newman, William G, Shore, Roger C, Brookes, Steven J, Mighell, Alan J, Inglehearn, Chris F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5026821/
https://www.ncbi.nlm.nih.gov/pubmed/27302843
http://dx.doi.org/10.1038/ejhg.2016.62

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5026821/
https://www.ncbi.nlm.nih.gov/pubmed/27302843
http://dx.doi.org/10.1038/ejhg.2016.62

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