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Identification of four novel mutations in classical menkes disease and successful prenatal DNA diagnosis Hahn, S; Cho, K; Ryu, K; Kim, J; Pai, K; Kim, M; Park, H; et al, MOLECULAR GENETICS AND METABOLISM, v.73, no.1, pp.86 - 90, 2001-05 |
Identification of three novel mutations and a high frequency of the Arg778Leu mutation in Korean patients with Wilson disease Kim, EK; Yoo, Ook-Joon; Song, KY; Yoo, HW; Choi, SY; Cho, SW; Hahn, SH, HUMAN MUTATION, v.11, no.4, pp.275 - 278, 1998 |
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