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Comment
. 2015 Sep;138(Pt 9):e377.
doi: 10.1093/brain/awv015. Epub 2015 Feb 12.

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

Sylvie Bannwarth  1 , Samira Ait-El-Mkadem  1 , Annabelle Chaussenot  1 , Emmanuelle C Genin  2 , Sandra Lacas-Gervais  3 , Konstantina Fragaki  1 , Laetitia Berg-Alonso  2 , Yusuke Kageyama  4 , Valérie Serre  5 , David Moore  6 , Annie Verschueren  7 , Cécile Rouzier  1 , Isabelle Le Ber  8 , Gaëlle Augé  1 , Charlotte Cochaud  9 , Françoise Lespinasse  2 , Karine N'Guyen  10 , Anne de Septenville  11 , Alexis Brice  11 , Patrick Yu-Wai-Man  12 , Hiromi Sesaki  4 , Jean Pouget  7 , Véronique Paquis-Flucklinger  13
Affiliations
Comment

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

Sylvie Bannwarth et al. Brain. 2015 Sep.
No abstract available

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References

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