DOK7 congenital myasthenia may be associated with severe mitral valve insufficiency

David Gaist*, Jens Mogensen, Emil Greve Pedersen, Henrik Daa Schrøder, John Vissing, Henning Andersen, Jens Michael Hertz

*Kontaktforfatter for dette arbejde

Publikation: Bidrag til tidsskriftKommentar/debatForskningpeer review

OriginalsprogEngelsk
TidsskriftJournal of the Neurological Sciences
Vol/bind379
Sider (fra-til)217-218
ISSN0022-510X
DOI
StatusUdgivet - 15. aug. 2017

Citer dette

@article{955a56e8636c4366980c9d21d1c3a322,
title = "DOK7 congenital myasthenia may be associated with severe mitral valve insufficiency",
keywords = "Cardiac disease, DOK7 congenital myasthenia, Mitral valve disease, Neuromuscular disorders, Myasthenic Syndromes, Congenital/complications, Muscle Proteins/genetics, Humans, Middle Aged, Genetic Predisposition to Disease/genetics, Male, Female, Mutation, Mitral Valve Insufficiency/complications, Siblings",
author = "David Gaist and Jens Mogensen and Pedersen, {Emil Greve} and Schr{\o}der, {Henrik Daa} and John Vissing and Henning Andersen and Hertz, {Jens Michael}",
year = "2017",
month = "8",
day = "15",
doi = "10.1016/j.jns.2017.06.005",
language = "English",
volume = "379",
pages = "217--218",
journal = "Journal of the Neurological Sciences",
issn = "0022-510X",
publisher = "Elsevier",

}

DOK7 congenital myasthenia may be associated with severe mitral valve insufficiency. / Gaist, David; Mogensen, Jens; Pedersen, Emil Greve; Schrøder, Henrik Daa; Vissing, John; Andersen, Henning; Hertz, Jens Michael.

I: Journal of the Neurological Sciences, Bind 379, 15.08.2017, s. 217-218.

Publikation: Bidrag til tidsskriftKommentar/debatForskningpeer review

TY - JOUR

T1 - DOK7 congenital myasthenia may be associated with severe mitral valve insufficiency

AU - Gaist, David

AU - Mogensen, Jens

AU - Pedersen, Emil Greve

AU - Schrøder, Henrik Daa

AU - Vissing, John

AU - Andersen, Henning

AU - Hertz, Jens Michael

PY - 2017/8/15

Y1 - 2017/8/15

KW - Cardiac disease

KW - DOK7 congenital myasthenia

KW - Mitral valve disease

KW - Neuromuscular disorders

KW - Myasthenic Syndromes, Congenital/complications

KW - Muscle Proteins/genetics

KW - Humans

KW - Middle Aged

KW - Genetic Predisposition to Disease/genetics

KW - Male

KW - Female

KW - Mutation

KW - Mitral Valve Insufficiency/complications

KW - Siblings

U2 - 10.1016/j.jns.2017.06.005

DO - 10.1016/j.jns.2017.06.005

M3 - Comment/debate

C2 - 28716243

AN - SCOPUS:85020895129

VL - 379

SP - 217

EP - 218

JO - Journal of the Neurological Sciences

JF - Journal of the Neurological Sciences

SN - 0022-510X

ER -