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Autor:
Thu T. Duong, Vidyullatha Vasireddy, Pavitra Ramachandran, Pamela S. Herrera, Lanfranco Leo, Carrie Merkel, Jean Bennett, Jason A. Mills
Publikováno v:
Stem Cell Research, Vol 27, Iss , Pp 140-150 (2018)
Choroideremia (CHM) is a rare monogenic, X-linked recessive inherited retinal degeneration resulting from mutations in the Rab Escort Protein-1 (REP1) encoding CHM gene. The primary retinal cell type leading to CHM is unknown. In this study, we explo
Externí odkaz:
https://doaj.org/article/cf3438c1f6194219b24035c1fd245aa0