Novel mutation in CNTNAP1 results in congenital hypomyelinating neuropathy.

Mehta P, Küspert M, Bale T, Brownstein CA, Towne MC, De Girolami U, Shi J, Beggs AH, Darras BT, Wegner M, Piao X, Agrawal PB (2017)

Publication Type: Journal article, Original article

Publication year: 2017

Journal

Muscle & Nerve Wiley-Blackwell

Pages Range: 761-765

Journal Issue: 55

DOI: 10.1002/mus.25416

Authors with CRIS profile

Melanie Küspert Lehrstuhl für Biochemie und Pathobiochemie Michael Wegner Lehrstuhl für Biochemie und Pathobiochemie

Involved external institutions

Harvard University US United States (USA) (US) City University of Hong Kong (CityU) CN China (CN)

How to cite

APA:

Mehta, P., Küspert, M., Bale, T., Brownstein, C.A., Towne, M.C., De Girolami, U.,... Agrawal, P.B. (2017). Novel mutation in CNTNAP1 results in congenital hypomyelinating neuropathy. Muscle & Nerve, 55, 761-765. https://dx.doi.org/10.1002/mus.25416

MLA:

Mehta, Paulomi, et al. "Novel mutation in CNTNAP1 results in congenital hypomyelinating neuropathy." Muscle & Nerve 55 (2017): 761-765.

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