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Automated sequencing has identified 70% of mutations in 30 patients with familial hypercholesterolaemia in Northern Ireland
C.A. Graham, A.J. Ward, N.C. Nevi, T. Trinick, I. Young, M. O'Kane, D.P. NichollsVolume:
112
Year:
1995
Language:
english
DOI:
10.1016/0021-9150(95)90026-8
File:
PDF, 122 KB
english, 1995