Mutations in the human SC4MOL gene encoding a methyl sterol oxidase cause psoriasiform dermatitis, microcephaly, and developmental delay-Reference-Cited by-同舟云学术

Mutations in the human SC4MOL gene encoding a methyl sterol oxidase cause psoriasiform dermatitis, microcephaly, and developmental delay

Published:2011-03-01 Issue:3 Volume:121 Page:976-984
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

He Miao,Kratz Lisa E.,Michel Joshua J.,Vallejo Abbe N.,Ferris Laura,Kelley Richard I.,Hoover Jacqueline J.,Jukic Drazen,Gibson K. Michael,Wolfe Lynne A.,Ramachandran Dhanya,Zwick Michael E.,Vockley Jerry

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference46 articles.

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4. Crosstalk between LXR and Toll-like Receptor Signaling Mediates Bacterial and Viral Antagonism of Cholesterol Metabolism

5. Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger-Huet anomaly

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