A case of autosomal recessive spinocerebellar ataxia type 18 with a novel mutation in GRID2

Hetzelt K, Kraus C, Kusnik S, Thiel C, Ekici AB, Reis A, Zweier C (2020)

Publication Type: Conference contribution

Publication year: 2020

Journal

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

Publisher: SPRINGERNATURE

City/Town: LONDON

Pages Range: 867-867

Conference Proceedings Title: EUROPEAN JOURNAL OF HUMAN GENETICS

Authors with CRIS profile

Katalin Blum Institute of Human Genetics Cornelia Kraus Institute of Human Genetics Stefan Kusnik Department of Paediatrics and Adolescent Medicine Arif Bülent Ekici Institute of Human Genetics André Wiesmann da Silva Reis Lehrstuhl für Humangenetik Christiane Zweier Medizinische Fakultät

How to cite

APA:

Hetzelt, K., Kraus, C., Kusnik, S., Thiel, C., Ekici, A.B., Reis, A., & Zweier, C. (2020). A case of autosomal recessive spinocerebellar ataxia type 18 with a novel mutation in GRID2. In EUROPEAN JOURNAL OF HUMAN GENETICS (pp. 867-867). LONDON: SPRINGERNATURE.

MLA:

Hetzelt, Katalin, et al. "A case of autosomal recessive spinocerebellar ataxia type 18 with a novel mutation in GRID2." Proceedings of the EUROPEAN JOURNAL OF HUMAN GENETICS LONDON: SPRINGERNATURE, 2020. 867-867.

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