Copy number analysis reveals a novel multiexon deletion of the colq gene in congenital myasthenia

Wei Wang, Yanhong Wu, Chen Wang, Jinsong Jiao, Christopher Jon Klein

Research output: Contribution to journalShort survey

1 Citation (Scopus)
Original languageEnglish (US)
Article numbere117
JournalNeurology: Genetics
Volume2
Issue number6
DOIs
StatePublished - Jan 1 2016

Fingerprint

Congenital Myasthenic Syndromes
Gene Deletion

ASJC Scopus subject areas

  • Clinical Neurology
  • Genetics(clinical)

Cite this

Copy number analysis reveals a novel multiexon deletion of the colq gene in congenital myasthenia. / Wang, Wei; Wu, Yanhong; Wang, Chen; Jiao, Jinsong; Klein, Christopher Jon.

In: Neurology: Genetics, Vol. 2, No. 6, e117, 01.01.2016.

Research output: Contribution to journalShort survey

@article{b972e0a5988d41808288ec6a67f489b8,
title = "Copy number analysis reveals a novel multiexon deletion of the colq gene in congenital myasthenia",
author = "Wei Wang and Yanhong Wu and Chen Wang and Jinsong Jiao and Klein, {Christopher Jon}",
year = "2016",
month = "1",
day = "1",
doi = "10.1212/NXG.0000000000000117",
language = "English (US)",
volume = "2",
journal = "Neurology: Genetics",
issn = "2376-7839",
publisher = "Lippincott Williams and Wilkins",
number = "6",

}

TY - JOUR

T1 - Copy number analysis reveals a novel multiexon deletion of the colq gene in congenital myasthenia

AU - Wang, Wei

AU - Wu, Yanhong

AU - Wang, Chen

AU - Jiao, Jinsong

AU - Klein, Christopher Jon

PY - 2016/1/1

Y1 - 2016/1/1

UR - http://www.scopus.com/inward/record.url?scp=85052668187&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=85052668187&partnerID=8YFLogxK

U2 - 10.1212/NXG.0000000000000117

DO - 10.1212/NXG.0000000000000117

M3 - Short survey

AN - SCOPUS:85052668187

VL - 2

JO - Neurology: Genetics

JF - Neurology: Genetics

SN - 2376-7839

IS - 6

M1 - e117

ER -