Smith-Lemli-Opitz syndrome is caused by mutations in the 7-dehydrocholesterol reductase gene
Publication year
1998Source
American Journal of Human Genetics, 63, 2, (1998), pp. 329-338ISSN
Publication type
Article / Letter to editor
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Organization
Neurophysiology
Radboudumc Extern
Paediatrics - OUD tm 2017
Neurology
Journal title
American Journal of Human Genetics
Volume
vol. 63
Issue
iss. 2
Page start
p. 329
Page end
p. 338
Subject
The Smith-Lemli-Opitz syndrome; Het Smith-Lemli-Opitz syndromeThis item appears in the following Collection(s)
- Academic publications [243179]
- Electronic publications [129863]
- Faculty of Medical Sciences [92416]
- Faculty of Science [36653]
- Open Access publications [104391]
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