| 1 | PHOX2A, 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
|
| 2 | PHOX2A, 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
|
| 3 | PHOX2A, 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
|
| 4 | FEOM2, 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
|
| 5 | FEOM2
|
| 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
|
| 6 | FEOM1, FEOM2
|
| Locus heterogeneity in autosomal dominant congenital external ophthalmoplegia (CFEOM).
|
| Black GCM, et al.
|
| J Med Genet 35 : 985-988. 1998
|
| 7 | FEOM2
|
| 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
|