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Tyson J., Tranebjaerg L., Bellman S., Wren C., Taylor J., Bathen J., Aslaksen B., Sorland S.J., Lund O., Malcolm S., Pembrey M., Bhattacharya S., Bitner-Glindzicz M. IsK and KvLQT1: mutation in either of the two components of the delayed rectifier potassium channel can cause the Jervell and Lange-Nielsen syndrome. - Am.J.Hum.Genet., 1997, v. 61 (suppl.), p. A349.
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