Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Fibrosis and KIF21A[original query] |
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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 |
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 |
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 |
Clinical and genetic characteristics of Chinese patients with congenital cranial dysinnervation disorders. Orphanet journal of rare diseases 2022 12 17 (1): 431. Jia Hongyan, Ma Qian, Liang Yi, Wang Dan, Chang Qinglin, Zhao Bo, Zhang Zongrui, Liang Jing, Song Jing, Wang Yidi, Zhang Ranran, Tu Zhanhan, Jiao Yongho |
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