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Publikováno v:
Acta Ophthalmologica. 86
Purpose To report the clinical and molecular findings in Polish patients with stromal corneal dystrophies caused by TGFBI gene mutations. Methods Patients with clinically diagnosed granular (n=14; 9 unrelated families) and lattice (n=2; 2 unrelated f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::57ce251e8e29f68090da623739c8b209
https://doi.org/10.1111/j.1755-3768.2008.480.x
https://doi.org/10.1111/j.1755-3768.2008.480.x
