Incidence and molecular mechanism of abberant splicing to a G->C splice acceptor site mutation causing Smith-Lemli-Opitz syndrome

Autor:	Waterham, H.R., Oostheim, W., Romeijn, G.J., Wanders, R.J.A., Hennekam, R.C.M.
Přispěvatelé:	Faculteit der Geneeskunde
Rok vydání:	2000
Zdroj:	Journal of Medical Genetics, 37, 389-392. BMJ Publishing Group
ISSN:	0022-2593
Databáze:	OpenAIRE
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