Clinical and genetic findings in a family with NMNAT1-associated Leber congenital amaurosis: case report and review of the literature
Wissenschaftlicher Artikel
Autoren
Hedergott, A.
Volk, A. E.
Herkenrath, P.
Thiele, H.
Fricke, J.
Institutionen
UKU. Institut für HumangenetikErschienen in
Graefes Archive for Clinical and Experimental Ophthalmology ; 253 (2015), 12. - S. 2239-2246. - ISSN 0721-832X. - eISSN 1435-702X