DHCR7 mutations in Brazilian Smith-Lemli-Opitz syndrome patients

descriptionPublicationkeyboard_double_arrow_right Article 01 Jan 2005 English Publisher:WileyJournal:American Journal of Medical Genetics Part A, volume 136A, pages 278-281 (issn: 1552-4825, eissn: 1552-4833,

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Authors: F B, Scalco; L S, Correa-Cerro; C A, Wassif; F D, Porter; D, Moretti-Ferreira;

doi: 10.1002/ajmg.a.30810

pmid: 15952211

DHCR7 mutations in Brazilian Smith-Lemli-Opitz syndrome patients

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Related Organizations

National Institute of Health
Pakistan
Sao Paulo State University
Brazil
National Institute of Child Health and Human Development
United States
National Institutes of Health
United States

Keywords

Oxidoreductases Acting on CH-CH Group Donors, Base Sequence, DNA Mutational Analysis, Mutation, Humans, DNA, Brazil, Smith-Lemli-Opitz Syndrome

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