J Clin Neurosci

Whole exome sequencing identifies novel variant underlying hereditary spastic paraplegia in consanguineous Pakistani families.

Zulfiqar S, Tariq M, Ali Z, ..., Dahl N, Baig SM

J Clin Neurosci 67 (-) 19-23 [2019-09-00; online 2019-07-04]

NGI Uppsala (Uppsala Genome Center) [Service] National Genomics Infrastructure [Service]