REFERENCES
- Gutowski NJ, Bosley TM, Engle EC. 110th ENMC International Workshop: the congenital cranial dysinnervation disorders (CCDDs): Naarden, The Netherlands, 25–27 October, 2002. Neuromuscul Disord. 2003;13:573–578.
- Iannaccone A, McIntosh N, Ciccarelli ML, Baldi A, Mutolo PA, Tedesco SA, Engle EC. Familial unilateral Brown syndrome. Ophthalmic Genet. 2002;23:175–184.
- Jiang Y, Matsuo T, Fujiwara H, Hasebe S, Ohtsuki H, Yasuda T. ARIX gene polymorphisms in patients with congenital superior oblique muscle palsy. Br J Ophthalmol. 2004;88:263–267.
- Jiang Y, Matsuo T, Fujiwara H, Hasebe S, Ohtsuki H, Yasuda T. ARIX and PHOX2B polymorphisms in patients with congenital superior oblique muscle palsy. Acta Med Okayama. 2005;59:55–62.
- Imai S, Matsuo T, Itoshima E, Ohtsuki H. Clinical Features, ARIX and PHOX2B Nucleotide Changes in Three Families with Congenital Superior Oblique Muscle Palsy. Acta Med Okayama. 2008;62:45–53.