Article info

other Versions

PDF
Original article
Dominant ELOVL1 mutation causes neurological disorder with ichthyotic keratoderma, spasticity, hypomyelination and dysmorphic features

Authors

  1. Correspondence to Professor Rafał Płoski, Department of Medical Genetics, Medical University of Warsaw, Warsaw 02-106, Poland; rploski{at}wp.pl
View Full Text

Citation

Kutkowska-Kaźmierczak A, Rydzanicz M, Chlebowski A, et al
Dominant ELOVL1 mutation causes neurological disorder with ichthyotic keratoderma, spasticity, hypomyelination and dysmorphic features

Publication history

  • Received November 17, 2017
  • Revised February 2, 2018
  • Accepted February 5, 2018
  • First published March 1, 2018.

Article Versions

Request permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.