Citations for
1PHOX2A, FEOM2
Neurological features of congenital fibrosis of the extraocular muscles type 2 with mutations in PHOX2A.
Bosley TM, Oystreck DT, Robertson RL, al Awad A, Abu-Amero K, Engle EC.
Brain 129(Pt 9):2363-74. Epub 2006 Jun 30. 2006
2PHOX2A, FEOM2
ARIX gene polymorphisms in patients with congenital superior oblique muscle palsy.
Jiang Y, Matsuo T, Fujiwara H, Hasebe S, Ohtsuki H, Yasuda T.
Br J Ophthalmol 88(2):263-7. 2004
3PHOX2A, FEOM2
A novel PHOX2A/ARIX mutation in an Iranian family with congenital fibrosis of extraocular muscles type 2 (CFEOM2).
Yazdani A, Chung DC, Abbaszadegan MR, Al-Khayer K, Chan WM, Yazdani M, Ghodsi K, Engle EC, Traboulsi EI.
Am J Ophthalmol 136(5):861-5. 2003
4FEOM2, PHOX2A
Homozygous mutations in ARIX(PHOX2A) result in congenital fibrosis of the extraocular muscles type 2.
Nakano M, Yamada K, Fain J, Sener EC, Selleck CJ, Awad AH, Zwaan J, Mullaney PB, Bosley TM, Engle EC.
Nat Genet 29(3):315-20. 2001
5FEOM2
Congenital fibrosis of the extraocular muscles type 2, an inherited exotropic strabismus fixus, maps to distal 11q13.
Wang SM, Zwaan J, Mullaney PB, Jabak MH, Al-Awad A, Beggs AH, Engle EC.
Am J Hum Genet 63 : 517-525. 1998
6FEOM1, FEOM2
Locus heterogeneity in autosomal dominant congenital external ophthalmoplegia (CFEOM).
Black GCM, et al.
J Med Genet 35 : 985-988. 1998
7FEOM2
Linkage and homozygosity mapping of a variant of congenital fibrosis of the extraocular muscles to chromosome 11q13.1. (abstr)
Engle EC, et al.
Am J Hum Genet 61 : A30. 1997