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Comment
. 2015 Sep;138(Pt 9):e376.
doi: 10.1093/brain/awv014. Epub 2015 Feb 12.

A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation

Delia Kurzwelly  1 , Stefanie Krüger  2 , Saskia Biskup  2 , Michael T Heneka  3
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Comment

A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation

Delia Kurzwelly et al. Brain. 2015 Sep.
No abstract available

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  • Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation.
    Bannwarth S, Ait-El-Mkadem S, Chaussenot A, Genin EC, Lacas-Gervais S, Fragaki K, Berg-Alonso L, Kageyama Y, Serre V, Moore D, Verschueren A, Rouzier C, Le Ber I, Augé G, Cochaud C, Lespinasse F, N'Guyen K, de Septenville A, Brice A, Yu-Wai-Man P, Sesaki H, Pouget J, Paquis-Flucklinger V. Bannwarth S, et al. Brain. 2015 Sep;138(Pt 9):e377. doi: 10.1093/brain/awv015. Epub 2015 Feb 12. Brain. 2015. PMID: 25681413 Free PMC article. No abstract available.

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