The Smith-Lemli-Opitz syndrome is caused by mutations in the 7-dehydrocholesterol reductase gene

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Title:	The Smith-Lemli-Opitz syndrome is caused by mutations in the 7-dehydrocholesterol reductase gene
Author(s):	Waterham, H.R.; Wijburg, F.A.; Hennekam, R.C.M.; Vreken, P.; Poll-The, B.T.; Dorland, L.; Duran, M.; Jira, P.E.; Smeitink, J.A.M. ; Wevers, R.A. ; Wanders, R.J.
Publication year:	1998
Source:	American Journal of Human Genetics, vol. 63, (1998), pp. 329-338
Number of Pages:	10 p.
ISSN:	0002-9297
DOI:	https://doi.org/10.1086/301982
Publication type:	Article / Letter to editor
Please use this identifier to cite or link to this item : http://hdl.handle.net/2066/188593
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Subject:	Clinical and biochemical aspects of the Smith-Opitz syndrome. Klinische en biochemische aspecten van het Smith-Lemli-Opitz syndroom.
Organization:	Neurophysiology Radboudumc Extern Paediatrics Neurology
Journal title:	American Journal of Human Genetics
Volume:	vol. 63
Page start:	p. 329
Page end:	p. 338