Whole exome sequencing identifies novel variant underlying hereditary spastic paraplegia in consanguineous Pakistani families-Reference-Cited by-同舟云学术

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

Published:2019-09 Issue: Volume:67 Page:19-23
ISSN:0967-5868
Container-title:Journal of Clinical Neuroscience
language:en
Short-container-title:Journal of Clinical Neuroscience

Author:

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

Funder

Higher Education Commission (HEC)

Swedish Research Council

Publisher

Elsevier BV

Subject

Physiology (medical),Neurology (clinical),Neurology,General Medicine,Surgery

Reference29 articles.

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3. Mutations in CYP2U1, DDHD2 and GBA2 genes are rare causes of complicated forms of hereditary spastic paraparesis;Citterio;J Neurol,2014

4. Hereditary motor and sensory neuropathies and hereditary spastic paraplegia: a magnetic stimulation study;Clays;Ann Neurol,1990

5. A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24. 3;De Michele;Am J Human Genet,1998

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3. Clinical and genetic characteristics of CYP2U1-associated hereditary spastic paraplegia in three children from China;2023-10-19

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