Open AccessAccommodative insufficiency in a patient with Prader–Willi syndrome and SNRPN gene mutation
Author(s) -
Piotr Kanclerz
Publication year - 2019
Publication title -
saudi journal of ophthalmology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.359
H-Index - 25
eISSN - 2542-6680
pISSN - 1319-4534
DOI - 10.1016/j.sjopt.2019.05.006
Subject(s) - medicine , genetics , pediatrics , gene mutation , mutation , gene , bioinformatics , biology
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom