Reply: To PMID 25428574

Manu Jokela¹, Sini Penttilä², Bjarne Udd^{3

4}

Affiliations

¹ Division of Clinical Neurosciences, Turku University Hospital, and University of Turku, Turku.
² Neuromuscular Research Center, University of Tampere and Tampere University Hospital, Tampere.
³ Department of Neurology, Vasa Central Hospital, Helsinki.
⁴ Folkhälsan Genetic Institute, University of Helsinki, Helsinki, Finland.

Comment

Manu Jokela et al. Ann Neurol. 2015 Nov.

. 2015 Nov;78(5):831-2.

doi: 10.1002/ana.24465. Epub 2015 Aug 31.

Manu Jokela¹, Sini Penttilä², Bjarne Udd^{3

4}

¹ Division of Clinical Neurosciences, Turku University Hospital, and University of Turku, Turku.
² Neuromuscular Research Center, University of Tampere and Tampere University Hospital, Tampere.
³ Department of Neurology, Vasa Central Hospital, Helsinki.
⁴ Folkhälsan Genetic Institute, University of Helsinki, Helsinki, Finland.

No abstract available

Comment on

Late onset spinal motor neuronopathy is caused by mutation in CHCHD10.
Penttilä S, Jokela M, Bouquin H, Saukkonen AM, Toivanen J, Udd B. Penttilä S, et al. Ann Neurol. 2015 Jan;77(1):163-72. doi: 10.1002/ana.24319. Epub 2014 Dec 12. Ann Neurol. 2015. PMID: 25428574
CHCHD10 mutations are not a common cause of SMN1-negative type III/IV spinal motor atrophy.
Morel G, Rouzier C, Chaussenot A, Ait-El-Mkadem S, Bannwarth S, Genin EC, Augé G, Chabrol B, Pouget J, Soriani MH, Sacconi S, Paquis-Flucklinger V. Morel G, et al. Ann Neurol. 2015 Nov;78(5):831. doi: 10.1002/ana.24464. Epub 2015 Aug 31. Ann Neurol. 2015. PMID: 26095063 No abstract available.