HuGE Literature Finder
Records 1-3
A microdeletion in the GRHL2 Gene in two unrelated patients with congenital fibrosis of the extra ocular muscles.
BMC research notes 2017 Nov 10 (1): 562. Abu-Amero Khaled K, Kondkar Altaf A, Khan Arif |
KIF21A mutation in two Chinese families with congenital fibrosis of the extraocular muscles type 1 and 3.
Molecular medicine reports 2016 Aug . Chen Jingchang, Ye Qingqing, Deng Daming, Yan Jianhua, Lin Houbian, Shen Tao, Lin Yi |
Mutation analysis of KIF21A in congenital fibrosis of the extraocular muscles (CFEOM) patients.
Ophthalmic genetics 2004 Dec 25 (4): 241-6. Tiab Leila, d'Allèves Manzi Violaine, Borruat François-Xavier, Munier Francis, Schorderet Dani |
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