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pro vyhledávání: '"Natalie M Nguyen"'
Autor:
Douglas Vollrath, Douglas Yasumura, Gillie Benchorin, Michael T Matthes, Wei Feng, Natalie M Nguyen, Cecilia D Sedano, Melissa A Calton, Matthew M LaVail
Publikováno v:
PLoS Genetics, Vol 11, Iss 12, p e1005723 (2015)
Inherited photoreceptor degenerations (IPDs) are the most genetically heterogeneous of Mendelian diseases. Many IPDs exhibit substantial phenotypic variability, but the basis is usually unknown. Mutations in MERTK cause recessive IPD phenotypes assoc
Externí odkaz:
https://doaj.org/article/19a3a470e84d47019d54bf619c2aa96c
Autor:
Melissa A. Calton, Gillie Benchorin, Wei Feng, Douglas Vollrath, Matthew M. LaVail, Michael T. Matthes, Douglas Yasumura, Natalie M. Nguyen, Cecilia D. Sedano
Publikováno v:
PLoS Genetics
PLoS genetics, vol 11, iss 12
PLoS Genetics, Vol 11, Iss 12, p e1005723 (2015)
PLoS genetics, vol 11, iss 12
PLoS Genetics, Vol 11, Iss 12, p e1005723 (2015)
Inherited photoreceptor degenerations (IPDs) are the most genetically heterogeneous of Mendelian diseases. Many IPDs exhibit substantial phenotypic variability, but the basis is usually unknown. Mutations in MERTK cause recessive IPD phenotypes assoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b5ace712435b7bd239665004f8a44f4
http://europepmc.org/articles/PMC4687644
http://europepmc.org/articles/PMC4687644