2 results for author:"Kraus H." in Literature citations
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| Late onset is common in best macular dystrophy associated with VMD2 gene mutations. Renner A.B., Tillack H., Kraus H., Kramer F., Mohr N., Weber B.H., Foerster M.H., Kellner U. Ophthalmology 112:586-592(2005) · Mapped (9) |
| Identification of a novel mutation in the ryanodine receptor gene (RYR1) in patients with malignant hyperthermia. Rueffert H., Kraus H., Olthoff D., Deutrich C., Froster U.G. Hum. Mutat. 17:238-238(2001) · UniProtKB (1) |