Whole exome sequencing identifies a heterozygous missense variant in the PRDM5 gene in a family with Axenfeld–Rieger syndrome
Crossref DOI link: https://doi.org/10.1007/s10048-015-0462-0
Published Online: 2015-10-21
Published Print: 2016-01
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Micheal, Shazia
Siddiqui, Sorath Noorani
Zafar, Saemah Nuzhat
Venselaar, Hanka
Qamar, Raheel
Khan, Muhammad Imran
den Hollander, Anneke I.
License valid from 2015-10-21