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

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.

Comment

Liedewei Van de Vondel et al. Brain. 2020.

. 2020 Dec 1;143(12):e105.

doi: 10.1093/brain/awaa345.

Liedewei Van de Vondel^{1

2}, Jonathan Baets^{1

2

3}, Danique Beijer^{1

2}

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.

No abstract available

Comment on

Nonsense mutations in alpha-II spectrin in three families with juvenile onset hereditary motor neuropathy.
Beijer D, Deconinck T, De Bleecker JL, Dotti MT, Malandrini A, Urtizberea JA, Zulaica M, López de Munain A, Asselbergh B, De Jonghe P, Baets J. Beijer D, et al. Brain. 2019 Sep 1;142(9):2605-2616. doi: 10.1093/brain/awz216. Brain. 2019. PMID: 31332438
De novo SPTAN1 mutation in axonal sensorimotor neuropathy and developmental disorder.
Ylikallio E, Ritari N, Sainio M, Toppila J, Kivirikko S, Tyynismaa H, Auranen M, Isohanni P. Ylikallio E, et al. Brain. 2020 Dec 1;143(12):e104. doi: 10.1093/brain/awaa344. Brain. 2020. PMID: 33206935 No abstract available.