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Human Molecular Genetics
|
October 24, 2015
Hypomorphic mutations in TRNT1 cause retinitis pigmentosa with erythrocytic microcytosis
Adam P DeLuca, S Scott Whitmore, Jenna Barnes, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
June 17, 2017
Using CRISPR-Cas9 to Generate Gene-Corrected Autologous iPSCs for the Treatment of Inherited Retinal Degeneration
Erin R Burnight, Manav Gupta, Luke A Wiley, et al.
Ophthalmology
|
October 29, 2015
North Carolina Macular Dystrophy Is Caused by Dysregulation of the Retinal Transcription Factor PRDM13
Kent W Small, Adam P DeLuca, S Scott Whitmore, et al.
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Search research articles
Search
Showing results (51-60 of 53) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 53 results.
Human Molecular Genetics
|
October 24, 2015
Hypomorphic mutations in TRNT1 cause retinitis pigmentosa with erythrocytic microcytosis
Adam P DeLuca, S Scott Whitmore, Jenna Barnes, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
June 17, 2017
Using CRISPR-Cas9 to Generate Gene-Corrected Autologous iPSCs for the Treatment of Inherited Retinal Degeneration
Erin R Burnight, Manav Gupta, Luke A Wiley, et al.
Ophthalmology
|
October 29, 2015
North Carolina Macular Dystrophy Is Caused by Dysregulation of the Retinal Transcription Factor PRDM13
Kent W Small, Adam P DeLuca, S Scott Whitmore, et al.
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of 6