Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Martyna, Smolińska"'
Autor:
Aneta, Ścieżyńska, Marta, Soszyńska, Michał, Komorowski, Anna, Podgórska, Natalia, Krześniak, Aleksandra, Nogowska, Martyna, Smolińska, Kamil, Szulborski, Jacek P, Szaflik, Bartłomiej, Noszczyk, Monika, Ołdak, Jacek, Malejczyk
Publikováno v:
International Journal of Molecular Sciences
ABCA4 gene mutations are the cause of a spectrum of ABCA4 retinopathies, and the most common juvenile macular degeneration is called Stargardt disease. ABCA4 has previously been observed almost exclusively in the retina. Therefore, studying the funct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d9ba1119ce9d2e41f8b881decda843eb
https://pubmed.ncbi.nlm.nih.gov/32413971
https://pubmed.ncbi.nlm.nih.gov/32413971
Autor:
Monika Ołdak, Aleksandra Nogowska, Bartłomiej Noszczyk, Kamil Szulborski, Martyna Smolińska, Anna Podgórska, Natalia Krześniak, Jacek P. Szaflik, Jacek Malejczyk, Michal Komorowski, Aneta Ścieżyńska, Marta Soszyńska
Publikováno v:
International Journal of Molecular Sciences
Volume 21
Issue 10
International Journal of Molecular Sciences, Vol 21, Iss 3430, p 3430 (2020)
Volume 21
Issue 10
International Journal of Molecular Sciences, Vol 21, Iss 3430, p 3430 (2020)
ABCA4 gene mutations are the cause of a spectrum of ABCA4 retinopathies, and the most common juvenile macular degeneration is called Stargardt disease. ABCA4 has previously been observed almost exclusively in the retina. Therefore, studying the funct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::972d650f14b882ca2e68239f005a58ae
https://doi.org/10.3390/ijms21103430
https://doi.org/10.3390/ijms21103430