Whole exome sequencing identifies a heterozygous missense variant in the PRDM5 gene in a family with Axenfeld–Rieger syndrome

Axenfeld–Rieger syndrome (ARS) is a disorder affecting the anterior segment of the eye, often leading to secondary glaucoma and several systemic malformations. It is inherited in an autosomal dominant fashion that has been associated with genetic defects in PITX2 and FOXC1. Known genes CYP1b1, PITX2...

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Detalles Bibliográficos
Autores principales: Micheal, Shazia, Siddiqui, Sorath Noorani, Zafar, Saemah Nuzhat, Venselaar, Hanka, Qamar, Raheel, Khan, Muhammad Imran, den Hollander, Anneke I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2015
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4701771/
https://www.ncbi.nlm.nih.gov/pubmed/26489929
http://dx.doi.org/10.1007/s10048-015-0462-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4701771/
https://www.ncbi.nlm.nih.gov/pubmed/26489929
http://dx.doi.org/10.1007/s10048-015-0462-0

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