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Page 1
Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1).
Yamada K, Andrews C, Chan WM, McKeown CA, Magli A, de Berardinis T, Loewenstein A, Lazar M, O'Keefe M, Letson R, London A, Ruttum M, Matsumoto N, Saito N, Morris L, Del Monte M, Johnson RH, Uyama E, Houtman WA, de Vries B, Carlow TJ, Hart BL, Krawiecki N, Shoffner J, Vogel MC, Katowitz J, Goldstein SM, Levin AV, Sener EC, Ozturk BT, Akarsu AN, Brodsky MC, Hanisch F, Cruse RP, Zubcov AA, Robb RM, Roggenkäemper P, Gottlob I, Kowal L, Battu R, Traboulsi EI, Franceschini P, Newlin A, Demer JL, Engle EC. Yamada K, et al. Among authors: houtman wa. Nat Genet. 2003 Dec;35(4):318-21. doi: 10.1038/ng1261. Epub 2003 Nov 2. Nat Genet. 2003. PMID: 14595441
Hereditary congenital external ophthalmoplegia.
Houtman WA, van Weerden TW, Robinson PH, de Vries B, Hoogenraad TU. Houtman WA, et al. Ophthalmologica. 1986;193(4):207-18. doi: 10.1159/000309712. Ophthalmologica. 1986. PMID: 3587876
Squint in monozygotic twins.
de Vries B, Houtman WA. de Vries B, et al. Among authors: houtman wa. Doc Ophthalmol. 1979 Mar 15;46(2):305-8. doi: 10.1007/BF00142619. Doc Ophthalmol. 1979. PMID: 573196
On the many faces of Leber hereditary optic neuropathy.
Oostra RJ, Tijmes NT, Cobben JM, Bolhuis PA, van Nesselrooij BP, Houtman WA, de Kok-Nazaruk MM, Bleeker-Wagemakers EM. Oostra RJ, et al. Among authors: houtman wa. Clin Genet. 1997 Jun;51(6):388-93. doi: 10.1111/j.1399-0004.1997.tb02496.x. Clin Genet. 1997. PMID: 9237501
Lacrimal sweating in a patient with Reader's syndrome.
van Weerden TW, Houtman WA, Schweitzer NM, Minderhoud JM. van Weerden TW, et al. Among authors: houtman wa. Clin Neurol Neurosurg. 1979;81(2):119-21. doi: 10.1016/s0303-8467(79)80022-0. Clin Neurol Neurosurg. 1979. PMID: 225078
28 results