Search

Author/Creator Zulfiqar, Shumaila

2. Whole exome sequencing identifies novel variant underlying hereditary spastic paraplegia in consanguineous Pakistani families. (September 2019)

Authors:
Zulfiqar, Shumaila; Tariq, Muhammad; Ali, Zafar; Fatima, Ambrin; Klar, Joakim; Abdullah, Uzma; Ali, Aamir; Ramzan, Shafaq; He, Sijie; Zhang, Jianguo; Khan, Ayaz; Shah, Suleman; Khan, Sheraz; Makhdoom, Ehtishamul Haq; Schuster, Jens; Dahl, Niklas; Baig, Shahid Mahmood
Journal:
Journal of clinical neuroscience
Issue:
Volume 67(2019)
Page Start:
19
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

Limit your search