Download Citation
Article Source:
Identification of Novel and Recurrent Disease-Causing Mutations in Retinal Dystrophies Using Whole Exome Sequencing (WES): Benefits and Limitations
Tiwari A,
Lemke J,
Altmueller J,
Thiele H,
Glaus E,
et al.
(2016)
Identification of Novel and Recurrent Disease-Causing Mutations in Retinal Dystrophies Using Whole Exome Sequencing (WES): Benefits and Limitations.
PLOS ONE 11(7): e0158692.
https://doi.org/10.1371/journal.pone.0158692