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Letter to the Editor

Mutations in KIF21A and PHOX2A are absent in 16 patients with congenital vertical incomitant strabismus

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Pages 206-207 | Received 21 Mar 2009, Accepted 11 Jul 2009, Published online: 23 Oct 2009

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.

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