Investigation of 7-dehydrocholesterol reductase pathway to elucidate off-target prenatal effects of pharmaceuticals: a systematic review

Mendelian diseases contain important biological information regarding developmental effects of gene mutations that can guide drug discovery and toxicity efforts. In this review, we focus on Smith–Lemli–Opitz syndrome (SLOS), a rare Mendelian disease characterized by compound heterozygous mutations i...

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Detalles Bibliográficos
Autores principales: Boland, M R, Tatonetti, N P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5028238/
https://www.ncbi.nlm.nih.gov/pubmed/27401223
http://dx.doi.org/10.1038/tpj.2016.48

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5028238/
https://www.ncbi.nlm.nih.gov/pubmed/27401223
http://dx.doi.org/10.1038/tpj.2016.48

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