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Human Molecular Genetics|April 2, 2014
Abnormal retinal development associated with FRMD7 mutationsMervyn G Thomas, Moira Crosier, Susan Lindsay, et al.Brain : a Journal of Neurology|February 10, 2011
The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmusMervyn G Thomas, Moira Crosier, Susan Lindsay, et al.Brain : a Journal of Neurology|March 29, 2008
Phenotypical characteristics of idiopathic infantile nystagmus with and without mutations in FRMD7Shery Thomas, Frank A Proudlock, Nagini Sarvananthan, et al.BMJ Open|August 3, 2026
Cerebrospinal fluid shunting or dural venous sinus stenting to preserve vision in idiopathic intracranial hypertension (IIH Intervention): protocol for an open-label, multicentre, randomised controlled phase IIb trialGeorgios Tsermoulas, Susan P Mollan, Victoria Homer, et al.Nature Genetics|October 3, 2006
Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmusPatrick Tarpey, Shery Thomas, Nagini Sarvananthan, et al.Pageof 2