Exome sequencing identifies a mutation in OFD1 in a male with Joubert syndrome, orofaciodigital spectrum anomalies and complex polydactyly

Orofaciodigital syndrome type 1 or oral–facial–digital syndrome type 1 (OFDS1, OMIM #311200) is an X-linked malformation syndrome caused by hemizygous mutations in the OFD1 (OMIM #300170) gene with presumed male lethality. Recently males with OFDS1 and mutations in OFD1 have been described. We repor...

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Detalles Bibliográficos
Autores principales: Wentzensen, Ingrid M, Johnston, Jennifer J, Patton, John H, Graham, John M, Sapp, Julie C, Biesecker, Leslie G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Data Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4760119/
https://www.ncbi.nlm.nih.gov/pubmed/27081566
http://dx.doi.org/10.1038/hgv.2015.69

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4760119/
https://www.ncbi.nlm.nih.gov/pubmed/27081566
http://dx.doi.org/10.1038/hgv.2015.69

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