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Neurologic phenotypes associated with COL4A1/2 mutations: Expanding the spectrum of disease.

Lookup NU author(s): Dr Rhys ThomasORCiD

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Author(s): Zagaglia S, Selch C, Nisevic JR, Mei D, Michalak Z, Hernandez L, Krithika S, Vezyroglou K, Varadkar SM, Pepler A, Biskup S, Leão M, Gärter J, Merkenschlager A, Jaksch M, Møller RS, Gardella E, Kristiansen BS, Hansen LK, Vari MS, Helbig KL, Desai S, SmithHicks CL, HinoFukuyo N, Talvik T, Laugesaar R, Ilves P, Õunap K, Körber I, Hartlieb T, Kudernatsch M, Winkler P, Schimmel M, Hasse A, Knuf M, Heinemeyer J, Makowski C, Ghedia S, Subramanian GM, Striano P, Thomas RH, Micallef C, Thom M, Werring DJ, Kluger GJ, Cross JH, Guerrini R, Balestrini S, Sisodiya SM

Publication type: Article

Publication status: Published

Journal: Neurology

Year: 2018

Volume: 91

Issue: 22

Pages: e2078-e2088

Online publication date: 09/11/2018

Acceptance date: 17/08/2018

Date deposited: 07/12/2018

ISSN (print): 0028-3878

ISSN (electronic): 1526-632X

Publisher: Wolters Kluwer Health

URL: https://doi.org/10.1212/WNL.0000000000006567

DOI: 10.1212/WNL.0000000000006567

PubMed id: 30413629

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