Reply: De novo SPTAN1 mutation in axonal sensorimotor neuropathy and developmental disorder

Brain. 2020 Dec 1;143(12):e105. doi: 10.1093/brain/awaa345.

Authors

Liedewei Van de Vondel^{1

2}, Jonathan Baets^{1

2

3}, Danique Beijer^{1

2}

Affiliations

¹ Translational Neurosciences, Faculty of Medicine and Health Sciences, University of Antwerp, Belgium.
² Laboratory of Neuromuscular Pathology, Institute Born-Bunge, University of Antwerp, Belgium.
³ Neuromuscular Reference Centre, Department of Neurology, Antwerp University Hospital, Belgium.

PMID: 33207363
DOI: 10.1093/brain/awaa345

No abstract available

Publication types

Letter
Comment

MeSH terms

Codon, Nonsense*
Humans
Peripheral Nervous System Diseases*
Phenotype
Spectrin

Substances

Codon, Nonsense
Spectrin