Reply: Genetic heterogeneity of neuronal intranuclear inclusion disease. What about the infantile variant?

Ann Clin Transl Neurol. 2021 Apr;8(4):1002-1004. doi: 10.1002/acn3.51330. Epub 2021 Mar 29.

Authors

Wai Yan Yau¹, Zhongbo Chen^{1

2}, Roisin Sullivan¹, Jana Vandrovcova¹, Henry Houlden^{1

3}

Affiliations

¹ Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, United Kingdom.
² Department of Neurodegenerative Diseases, UCL Queen Square Institute of Neurology, University College London, London, United Kingdom.
³ Neurogenetics Unit, National Hospital for Neurology and Neurosurgery, London, United Kingdom.

No abstract available

Publication types

Letter
Research Support, Non-U.S. Gov't
Comment

MeSH terms

Genetic Heterogeneity*
Humans
Intranuclear Inclusion Bodies
Neurodegenerative Diseases* / genetics

Supplementary concepts

Neuronal intranuclear inclusion disease

Grants and funding