MAPT p.V363I mutation A rare cause of corticobasal degeneration

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MAPT p.V363I mutation A rare cause of corticobasal degeneration

Author: Ahmed, Sarah; Fairen, Monica Diez; Sabir, Marya S.; Pastor, Pau; Ding, Jinhui; Ispierto, Lourdes; Butala, Ankur; Morris, Christopher M.; Schulte, Claudia; Gasser, Thomas; Jabbari, Edwin; Pletnikova, Olga; Morris, Huw R.; Troncoso, Juan; Gelpi, Ellen; Pantelyat, Alexander; Scholz, Sonja W.
Tübinger Autor(en):
Schulte, Claudia
Gasser, Thomas
Published in: Neurology - Genetics (2019), Bd. 5, Article UNSP e347
Verlagsangabe: Lippincott Williams & Wilkins
Language: English
Full text: http://dx.doi.org/10.1212/NXG.0000000000000347
ISSN: 2376-7839
DDC Classifikation: 570 - Life sciences; biology
610 - Medicine and health
Dokumentart: Article
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