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Congenital fibrosis syndrome associated with central nervous system abnormalities.
A novel PHOX2A/ARIX mutation in an Iranian family with congenital fibrosis of extraocular muscles type 2 (CFEOM2).
Genes, brainstem development, and eye movements.
CFEOM3: a new extraocular congenital fibrosis syndrome that maps to 16q24.2-q24.3.
Clinical features associated with an I126M alpha2-chimaerin mutation in a family with autosomal-dominant Duane retraction syndrome.
Congenital fibrosis of the extraocular muscles associated with cortical dysplasia and maldevelopment of the basal ganglia.
KIF21A mutations in two Chinese families with congenital fibrosis of the extraocular muscles (CFEOM).
Synergistic divergence: a distinct ocular motility dysinnervation pattern.
Neurological features of congenital fibrosis of the extraocular muscles type 2 with mutations in PHOX2A.
Human CFEOM1 mutations attenuate KIF21A autoinhibition and cause oculomotor axon stalling.
Diagnostic distinctions and genetic analysis of patients diagnosed with moebius syndrome.
Birth Defects: Moebius syndrome and related facial weakness disorders
Genetic Etiologies of Horizontal Strabismus
Genetic and anatomic basis of the fibrosis syndromes
Ocular Motor Nerve Development in the Presence and Absence of Extraocular Muscle.
Ex Vivo Oculomotor Slice Culture from Embryonic GFP-Expressing Mice for Time-Lapse Imaging of Oculomotor Nerve Outgrowth.