Clinical spectrum of 4H leukodystrophy caused by POLR3A and POLR3B mutations

Authors

Nicole I. Wolf
Adeline Vanderver, George Washington University
Rosalina M. van Spaendonk
Raphael Schiffmann
Bernard Brais
+17 additional authors

Document Type

Response or Comment

Publication Date

11-2014

Journal

Neurology

Volume

Volume 83, Issue 21

Inclusive Pages

1898-1905

Keywords

Hereditary Central Nervous System Demyelinating Diseases--diagnosis; Hereditary Central Nervous System Demyelinating Diseases--genetics; Mitochondrial Diseases--diagnosis; Mitochondrial Diseases--genetics; Mutation--genetics; RNA Polymerase III--genetics

Comments

Comment in

Little folks, little myelin, and little teeth. [Neurology. 2014]

PMCID: PMC4248461 [Available on 2015/5/18]

APA Citation

Wolf, N.I., Vanderver, A., van Spaendonk, R.M., Schiffman, R., Brais, B. et al. (2014). Clinical spectrum of 4H leukodystrophy caused by POLR3A and POLR3B mutations. Neurology, 83(21), 1898-1905.

Peer Reviewed

1