DOI:
10.1055/s-00000036
Laryngo-Rhino-Otologie
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References
Wehner LE, Folz BJ, Argyriou L, Twelkemeyer S, Teske U, Geisthoff UW, Werner JA, Engel W, Nayernia K.
Mutation analysis in hereditary haemorrhagic telangiectasia in Germany reveals 11 novel ENG and 12 novel ACVRL1/ALK1 mutations.
Clin Genet 2006; 69 ((3)) 239-245
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