Retinal structure, function and genetics in inherited and aquired retinal degenerative disease

Projekt: Avhandling

Status	Pågående
Gällande start-/slutdatum	2017/10/07 → …

Danon disease presenting with early onset of hypertrophic cardiomyopathy and peripheral pigmentary retinal dystrophy in a female with a de novo novel mosaic mutation in the LAMP2 gene
Meinert, M., Englund, E., Hedberg-Oldfors, C., Oldfors, A., Kornhall, B., Lundin, C. & Wittström, E., 2019 juli 2, I: Ophthalmic Genetics. 40, 3, s. 227–236 11 s.
Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift › Peer review

Öppen tillgång
Clinical, optical coherence tomography, and fundus autofluorescence findings in patients with intraocular tumors
Samuelsson, D., Sznage, M., Engelsberg, K. & Wittström, E., 2016, I: Clinical Ophthalmology. 10, s. 1953-1964 12 s.
Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift › Peer review

Öppen tillgång

Projektinformation