Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Matthew Brumm"'
Autor:
Jacque L. Duncan, Niamh B. Stover, Sharon B. Schwartz, Mohammad Othman, Barbara J. Jennings, K. Thiran Jayasundera, Richard G. Weleber, Alessandro Iannaccone, Karmen M Trzupek, Paul A. Sieving, Samuel G. Jacobson, John R. Heckenlively, Matthew Brumm, Sten Andréasson, Richard A. Lewis, Maria Laura Ciccarelli, Beverly M. Yashar, Kari Branham, Jean Bennett, Dianna K H Wheaton, Gerald A. Fishman, David G. Birch, Pelin Atmaca-Sonmez, Anand Swaroop, Athanasios J. Karoukis
Publikováno v:
Investigative ophthalmology & visual science, vol 53, iss 13
PURPOSE. To determine the proportion of male patients presenting simplex retinal degenerative disease (RD: retinitis pigmentosa [RP] or cone/cone-rod dystrophy [COD/CORD]) with mutations in the X-linked retinal degeneration genes RPGR and RP2. METHOD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b5ab545ef75fe898736dd04e69c37fe
https://escholarship.org/uc/item/4hv0g66m
https://escholarship.org/uc/item/4hv0g66m
