Exome sequencing is a useful diagnostic tool for complicated forms of hereditary spastic paraplegia

C. Bettencourt, J.L. Lopez-Sendon, J. Garcia-Caldentey, P. Rizzu, I.M.C. Bakker, O. Shomroni, B. Quintans, J.R. Davila, M.R. Bevova, M.J. Sobrido, P. Heutink, J.G. Yebenes

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)154-158
JournalClinical Genetics
Volume85
Issue number2
DOIs
Publication statusPublished - 2014

Cite this

Bettencourt, C., Lopez-Sendon, J. L., Garcia-Caldentey, J., Rizzu, P., Bakker, I. M. C., Shomroni, O., ... Yebenes, J. G. (2014). Exome sequencing is a useful diagnostic tool for complicated forms of hereditary spastic paraplegia. Clinical Genetics, 85(2), 154-158. https://doi.org/10.1111/cge.12133