J Clin Neurosci

ISSN	1532-2653
ISSN-L	0967-5868
IUID	c7c5434e3c1c4ea79acaacd1ccfc906f
Modified	2020-11-27T13:14:04.804Z
Created	2019-11-23T07:14:06.944Z

Year 2019

PubMed DOI Crossref

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]

SciLifeLab Data Centre

Publications 9.5.1