Skip to main content
Advertisement
Neurology.org
Journals
Neurology
Clinical Practice
Genetics
Neuroimmunology & Neuroinflammation
Specialty Sites
Equity, Diversity, and Inclusion
Innovations in Care Delivery
Without Borders
Collections
Topics A-Z
Residents & Fellows
Infographics
Patient Pages
Null Hypothesis
Translations
Podcast
CME
About
About the Journals
Contact Us
Editorial Board
Authors
Submit a Manuscript
Author Center
Advanced Search
Search for this keyword
Main menu
Neurology.org
Journals
Neurology
Clinical Practice
Genetics
Neuroimmunology & Neuroinflammation
Specialty Sites
Equity, Diversity, and Inclusion
Innovations in Care Delivery
Without Borders
Collections
Topics A-Z
Residents & Fellows
Infographics
Patient Pages
Null Hypothesis
Translations
Podcast
CME
About
About the Journals
Contact Us
Editorial Board
Authors
Submit a Manuscript
Author Center
Home
Articles
Issues
User menu
My Alerts
Log in
Search
Search for this keyword
Advanced search
A peer-reviewed clinical and translational neurology open access journal
My Alerts
Log in
Home
Articles
Issues
Alrohaif
,
Hadil
et al
"Whole-exome sequencing identifies mutations in
MYMK
in a mild form of Carey-Fineman-Ziter syndrome."
Neurology Genetics
4
.
2
(2018):
e226
.
Web. 27 Jan. 2021.
Citation Manager Formats
BibTeX
Bookends
EasyBib
EndNote (tagged)
EndNote 8 (xml)
Medlars
Mendeley
Papers
RefWorks Tagged
Ref Manager
RIS
Zotero