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Mutations in the Human Sterol Δ7-Reductase Gene at 11q12-13 Cause Smith-Lemli-Opitz Syndrome
1998
423 citations
Journal Article
bronze Open Access
Field-Weighted Citation Impact:
32.43
Mutations in the Human Sterol Δ7-Reductase Gene at 11q12-13 Cause Smith-Lemli-Opitz Syndrome | Researchclopedia
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Oregon Health & Science University
Forbes D. Porter
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National Institutes of Health