Retinoic acid catabolizing enzyme CYP 26C1 is a genetic modifier in SHOX deficiency-Reference-Cited by-同舟云学术

Retinoic acid catabolizing enzyme CYP 26C1 is a genetic modifier in SHOX deficiency

Published:2016-11-14 Issue:12 Volume:8 Page:1455-1469
ISSN:1757-4676
Container-title:EMBO Molecular Medicine
language:en
Short-container-title:EMBO Mol Med

Author:

Montalbano Antonino¹,Juergensen Lonny²,Roeth Ralph¹,Weiss Birgit¹,Fukami Maki³,Fricke‐Otto Susanne⁴,Binder Gerhard⁵,Ogata Tsutomu⁶,Decker Eva⁷,Nuernberg Gudrun⁸⁹,Hassel David²,Rappold Gudrun A¹¹⁰^ORCID

Affiliation:

1. Department of Human Molecular Genetics Heidelberg University Heidelberg Germany

2. Department of Internal Medicine III ‐ Cardiology Heidelberg University Hospital Heidelberg Germany

3. Department of Molecular Endocrinology National Research Institute for Child Health and Development Tokyo Japan

4. Children's Hospital Krefeld Krefeld Germany

5. Children's Hospital University of Tübingen Tübingen Germany

6. Department of Pediatrics Hamamatsu University School of Medicine Hamamatsu Japan

7. Bioscientia Center for Human Genetics Ingelheim Germany

8. Center for Molecular Medicine Cologne Germany

9. Cologne Center for Genomics Cologne Germany

10. Interdisciplinary Centre for Neurosciences (IZN) University of Heidelberg Heidelberg Germany

Funder

Deutsche Forschungsgemeinschaft

Universität Heidelberg

Deutsches Zentrum für Herz-Kreislaufforschung

Publisher

EMBO

Subject

Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.15252/emmm.201606623

Reference73 articles.

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