Novel hemizygous nonsense mutation in DRP2 is associated with inherited neuropathy

Ricardo H. Roda; Brett A. McCray; Christopher J. Klein; Ahmet Hoke

doi:10.1212/NXG.0000000000000220

Novel hemizygous nonsense mutation in DRP2 is associated with inherited neuropathy

Ricardo H. Roda, Brett A. McCray, Christopher J. Klein, Ahmet Hoke

School of Medicine

Research output: Contribution to journal › Article › peer-review

1 Scopus citations

Original language	English (US)
Article number	e220
Journal	Neurology: Genetics
Volume	4
Issue number	1
DOIs	https://doi.org/10.1212/NXG.0000000000000220
State	Published - Feb 1 2018

ASJC Scopus subject areas

Clinical Neurology
Genetics(clinical)

Access to Document

10.1212/NXG.0000000000000220

Cite this

@article{cb4d085eddcd453cae8ce4051706bb75,

title = "Novel hemizygous nonsense mutation in DRP2 is associated with inherited neuropathy",

author = "Roda, {Ricardo H.} and McCray, {Brett A.} and Klein, {Christopher J.} and Ahmet Hoke",

note = "Funding Information: The Article Processing Charge was funded by the authors.",

year = "2018",

month = feb,

day = "1",

doi = "10.1212/NXG.0000000000000220",

language = "English (US)",

volume = "4",

journal = "Neurology: Genetics",

issn = "2376-7839",

publisher = "Lippincott Williams and Wilkins",

number = "1",

}

TY - JOUR

T1 - Novel hemizygous nonsense mutation in DRP2 is associated with inherited neuropathy

AU - Roda, Ricardo H.

AU - McCray, Brett A.

AU - Klein, Christopher J.

AU - Hoke, Ahmet

N1 - Funding Information: The Article Processing Charge was funded by the authors.

PY - 2018/2/1

Y1 - 2018/2/1

UR - http://www.scopus.com/inward/record.url?scp=85048722175&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=85048722175&partnerID=8YFLogxK

U2 - 10.1212/NXG.0000000000000220

DO - 10.1212/NXG.0000000000000220

M3 - Article

C2 - 29473052

AN - SCOPUS:85048722175

SN - 2376-7839

VL - 4

JO - Neurology: Genetics

JF - Neurology: Genetics

IS - 1

M1 - e220

ER -

Novel hemizygous nonsense mutation in DRP2 is associated with inherited neuropathy

ASJC Scopus subject areas

Access to Document

Other files and links

Cite this