Smith-Lemli-Opitz syndrome: evidence of T93M as a common...

European Journal of Human Genetics 1999 Vol. 7; Iss. 8

Smith-Lemli-Opitz syndrome: evidence of T93M as a common mutation of Δ7-sterol reductase in Italy and report of three novel mutations

Ambruzzi, M A, Zelante, L, Ciccodicola, A, De Brasi, D, Esposito, T, Rossi, M, Parenti, G, Sperandeo, M P, Zuppaldi, A, Bardaro, T
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Volume:
7
Year:
1999
Language:
english
Pages:
4
DOI:
10.1038/sj.ejhg.5200390
File:
PDF, 336 KB
english, 1999
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