Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Astuti, G.D."'
Autor:
Siemiatkowska, A.M., Arimadyo, K., Moruz, L.M., Astuti, G.D., de Castro-Miró, M., Zonneveld, M.N., Strom, T.M., de Wijs, I.J., Hoefsloot, L.H., Faradz, S.M., Cremers, F.P., den Hollander, A.I., Collin, R.W.
Publikováno v:
Molecular Vision
ResearcherID
Molecular Vision, 17, pp. 3013-24
Molecular Vision, 17, 3013-24
Mol. Vis. 17, 3013-3024 (2011)
ResearcherID
Molecular Vision, 17, pp. 3013-24
Molecular Vision, 17, 3013-24
Mol. Vis. 17, 3013-3024 (2011)
Contains fulltext : 98108.pdf (Publisher’s version ) (Open Access) PURPOSE: Retinitis pigmentosa (RP) is a clinically and genetically heterogeneous retinal disorder. Despite tremendous knowledge about the genes involved in RP, little is known about
Autor:
Siemiatkowska, A.M., Astuti, G.D., Arimadyo, K., den Hollander, A.I., Faradz, S.M., Cremers, F.P., Collin, R.W.J.
Publikováno v:
Molecular Vision, 18, 2411-9
Molecular Vision, 18, pp. 2411-9
Molecular Vision, 18, pp. 2411-9
Contains fulltext : 108199.pdf (Publisher’s version ) (Open Access) PURPOSE: The purpose of this study was to identify the underlying molecular genetic defect in an Indonesian family with three affected individuals who had received a diagnosis of r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1c73a7290fd506f65eaacb52d87759c0
http://hdl.handle.net/2066/108199
http://hdl.handle.net/2066/108199