Mutation analysis in hereditary haemorrhagic telangiectasia in Germany reveals 11 novel ENG and 12 novel ACVRL1/ALK1 mutations
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W. Engel | K. Nayernia | Werner Ja | L. Wehner | U. Geisthoff | U. Teske | L. Argyriou | B. Folz | S. Twelkemeyer | J. Werner | W. Engel | Folz Bj | Stefan Twelkemeyer | Geisthoff Uw