Reply: Evaluation of exome sequencing variation in undiagnosed ataxias

Affiliations

¹ Institute of Genetic Medicine, Newcastle University, NE1 3BZ, UK.
² Institute of Genetic Medicine, Newcastle University, NE1 3BZ, UK p.f.chinnery@ncl.ac.uk.

Comment

Angela Pyle et al. Brain. 2015 Oct.

. 2015 Oct;138(Pt 10):e384.

doi: 10.1093/brain/awv088. Epub 2015 Apr 4.

¹ Institute of Genetic Medicine, Newcastle University, NE1 3BZ, UK.
² Institute of Genetic Medicine, Newcastle University, NE1 3BZ, UK p.f.chinnery@ncl.ac.uk.

No abstract available

Comment on

Exome sequencing in undiagnosed inherited and sporadic ataxias.
Pyle A, Smertenko T, Bargiela D, Griffin H, Duff J, Appleton M, Douroudis K, Pfeffer G, Santibanez-Koref M, Eglon G, Yu-Wai-Man P, Ramesh V, Horvath R, Chinnery PF. Pyle A, et al. Brain. 2015 Feb;138(Pt 2):276-83. doi: 10.1093/brain/awu348. Epub 2014 Dec 12. Brain. 2015. PMID: 25497598 Free PMC article.
Evaluation of exome sequencing variation in undiagnosed ataxias.
Sandford E, Li JZ, Burmeister M. Sandford E, et al. Brain. 2015 Oct;138(Pt 10):e383. doi: 10.1093/brain/awv087. Epub 2015 Apr 4. Brain. 2015. PMID: 25842391 Free PMC article. No abstract available.