Coexisting variants in OSTM1 and MANEAL cause a complex neurodegenerative disorder with NBIA-like brain abnormalities

Erstveröffentlichung

2017

Authors

Herebian, Diran

Alhaddad, Bader

Seibt, Annette

Schwarzmayr, Thomas

Danhauser, Katharina

et al.

Wissenschaftlicher Artikel

Published in

European Journal of Human Genetics ; 25 (2017), 9. - S. 1092-1095. - ISSN 1018-4813. - eISSN 1476-5438

Link to publication

https://dx.doi.org/10.1038/ejhg.2017.96

Institutions

UKU. Klinik für Kinder- und Jugendmedizin

Subject headings

[Free subject headings]: mutations | pde6b | iron
[DDC subject group]: DDC 610 / Medicine & health

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Metadata

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