The L450P mutation in KCND3 brings spinocerebellar ataxia and Brugada syndrome closer together

Anna Duarri; Esther Nibbeling; Michiel R. Fokkens; Michel Meijer; Erik Boddeke; Emmeline Lagrange; Giovanni Stevanin; Alexis Brice; Alexandra Durr; Dineke S. Verbeek

doi:10.1007/s10048-013-0370-0

The L450P mutation in KCND3 brings spinocerebellar ataxia and Brugada syndrome closer together

Anna Duarri, Esther Nibbeling, Michiel R. Fokkens, Michel Meijer, Erik Boddeke, Emmeline Lagrange, Giovanni Stevanin, Alexis Brice, Alexandra Durr, Dineke S. Verbeek^*

^*Corresponding author voor dit werk

Translational Immunology Groningen (TRIGR)

Onderzoeksoutput › Academic › peer review

17 Citaten (Scopus)

Originele taal-2	English
Pagina's (van-tot)	257-258
Aantal pagina's	2
Tijdschrift	Neurogenetics
Volume	14
Nummer van het tijdschrift	3-4
DOI's	https://doi.org/10.1007/s10048-013-0370-0
Status	Published - nov.-2013

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@article{7fd982e1e4194079b75ddb99dbdccfdb,

title = "The L450P mutation in KCND3 brings spinocerebellar ataxia and Brugada syndrome closer together",

keywords = "Adult, Brugada Syndrome, Female, Humans, Male, Middle Aged, Mutation, Shal Potassium Channels, Spinocerebellar Ataxias",

author = "Anna Duarri and Esther Nibbeling and Fokkens, {Michiel R.} and Michel Meijer and Erik Boddeke and Emmeline Lagrange and Giovanni Stevanin and Alexis Brice and Alexandra Durr and Verbeek, {Dineke S.}",

year = "2013",

month = nov,

doi = "10.1007/s10048-013-0370-0",

language = "English",

volume = "14",

pages = "257--258",

journal = "Neurogenetics",

issn = "1364-6745",

publisher = "Springer",

number = "3-4",

}

TY - JOUR

T1 - The L450P mutation in KCND3 brings spinocerebellar ataxia and Brugada syndrome closer together

AU - Duarri, Anna

AU - Nibbeling, Esther

AU - Fokkens, Michiel R.

AU - Meijer, Michel

AU - Boddeke, Erik

AU - Lagrange, Emmeline

AU - Stevanin, Giovanni

AU - Brice, Alexis

AU - Durr, Alexandra

AU - Verbeek, Dineke S.

PY - 2013/11

Y1 - 2013/11

KW - Adult

KW - Brugada Syndrome

KW - Female

KW - Humans

KW - Male

KW - Middle Aged

KW - Mutation

KW - Shal Potassium Channels

KW - Spinocerebellar Ataxias

U2 - 10.1007/s10048-013-0370-0

DO - 10.1007/s10048-013-0370-0

M3 - Comment/Letter to the editor

C2 - 23963749

SN - 1364-6745

VL - 14

SP - 257

EP - 258

JO - Neurogenetics

JF - Neurogenetics

IS - 3-4

ER -