3 results for author:"Rochels R." in Literature citations
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| A novel keratin 12 mutation in a German kindred with Meesmann's corneal dystrophy. Corden L.D., Swensson O., Swensson B., Rochels R., Wannke B., Thiel H.J., McLean W.H.I. Br. J. Ophthalmol. 84:527-530(2000) · UniProtKB (1) |
| Molecular genetics of Meesmann's corneal dystrophy: ancestral and novel mutations in keratin 12 (K12) and complete sequence of the human KRT12 gene. Corden L.D., Swensson O., Swensson B., Smith F.J.D., Rochels R., Uitto J., McLean W.H.I. Exp. Eye Res. 70:41-49(2000) · UniProtKB (1) |
| Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophy. Irvine A.D., Corden L.D., Swensson O., Swensson B., Moore J.E., Frazer D.G., Smith F.J.D., Knowlton R.G., Christophers E., Rochels R. et al. |