A novelHSD17B10mutation impairing the activities of the mitochondrial RNase P complex causes X-linked intractable epilepsy and neurodevelopmental regression-Reference-Cited by-同舟云学术

A novelHSD17B10mutation impairing the activities of the mitochondrial RNase P complex causes X-linked intractable epilepsy and neurodevelopmental regression

Published:2016-03-07 Issue:5 Volume:13 Page:477-485
ISSN:1547-6286
Container-title:RNA Biology
language:en
Short-container-title:RNA Biology

Author:

Falk Marni J.,Gai Xiaowu,Shigematsu Megumi,Vilardo Elisa,Takase Ryuichi,McCormick Elizabeth,Christian Thomas,Place Emily,Pierce Eric A.,Consugar Mark,Gamper Howard B.,Rossmanith Walter,Hou Ya-Ming

Publisher

Informa UK Limited

Subject

Cell Biology,Molecular Biology

Link

http://www.tandfonline.com/doi/pdf/10.1080/15476286.2016.1159381

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3. Human Brain Short Chain l-3-Hydroxyacyl Coenzyme A Dehydrogenase Is a Single-domain Multifunctional Enzyme

4. Type 10 17beta-hydroxysteroid dehydrogenase catalyzing the oxidation of steroid modulators of γ-aminobutyric acid type A receptors

5. Intracellular oxidation of allopregnanolone by human brain type 10 17beta-hydroxysteroid dehydrogenase

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