Functional missense and splicing variants in the retinoic acid catabolizing enzyme CYP26C1 in idiopathic short stature

Rappold GA, Montalbano A, Juergensen L, Fukami M, Thiel C, Hauer N, Roeth R, Weiss B, Naiki Y, Ogata T, Hassel D (2019)

Publication Type: Conference contribution

Publication year: 2019

Journal

European Journal of Human Genetics Nature Publishing Group: Open Access Hybrid Model Option B

Publisher: NATURE PUBLISHING GROUP

City/Town: LONDON

Pages Range: 129-130

Conference Proceedings Title: EUROPEAN JOURNAL OF HUMAN GENETICS

Event location: Milan, ITALY

DOI: 10.1038/s41431-018-0148-9

Authors with CRIS profile

Christian Thiel Medizinische Fakultät Nadine Hauer Lehrstuhl für Humangenetik

Involved external institutions

Ruprecht-Karls-Universität Heidelberg DE Germany (DE) National Center for Child Health and Development JP Japan (JP) Hamamatsu University / 浜松大学 JP Japan (JP)

How to cite

APA:

Rappold, G.A., Montalbano, A., Juergensen, L., Fukami, M., Thiel, C., Hauer, N.,... Hassel, D. (2019). Functional missense and splicing variants in the retinoic acid catabolizing enzyme CYP26C1 in idiopathic short stature. In EUROPEAN JOURNAL OF HUMAN GENETICS (pp. 129-130). Milan, ITALY: LONDON: NATURE PUBLISHING GROUP.

MLA:

Rappold, G. A., et al. "Functional missense and splicing variants in the retinoic acid catabolizing enzyme CYP26C1 in idiopathic short stature." Proceedings of the 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, ITALY LONDON: NATURE PUBLISHING GROUP, 2019. 129-130.

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