Results
|
1.
|
|
|
2.
|
|
|
3.
|
Recessive hereditary motor and sensory neuropathy caused by IGHMBP2 gene mutation. [electronic resource] by
- Shi, Chang-He
- Song, Bo
- Luo, Hai-Yang
- Mao, Cheng-Yuan
- Shang, Dan-Dan
- Cao, Yuan
- Sun, Shi-Lei
- Wu, Jun
- Zhuang, Zheng-Ping
- Xu, Yu-Ming
Producer: 20151102
In:
Neurology vol. 85
Availability: No items available.
|
|
4.
|
Two Novel Mutations and a [electronic resource] by
- Li, Yu-Sheng
- Yang, Zhi-Hua
- Zhang, Yao
- Yang, Jing
- Shang, Dan-Dan
- Zhang, Shu-Yu
- Wu, Jun
- Ji, Yan
- Zhao, Lu
- Shi, Chang-He
- Xu, Yu-Ming
Publication details: Aging and disease Aug 2019
In:
Aging and disease vol. 10
Availability: No items available.
|
|
5.
|
Genotype-phenotype correlation in a cohort of paroxysmal kinesigenic dyskinesia cases. [electronic resource] by
- Mao, Cheng-Yuan
- Shi, Chang-He
- Song, Bo
- Wu, Jun
- Ji, Yan
- Qin, Jie
- Li, Yu-Sheng
- Wang, Jing-Jing
- Shang, Dan-Dan
- Sun, Shi-Lei
- Xu, Yu-Ming
Producer: 20141222
In:
Journal of the neurological sciences vol. 340
Availability: No items available.
|
|
6.
|
A novel RAB39B gene mutation in X-linked juvenile parkinsonism with basal ganglia calcification. [electronic resource] by
- Shi, Chang-He
- Zhang, Shu-Yu
- Yang, Zhi-Hua
- Yang, Jing
- Shang, Dan-Dan
- Mao, Cheng-Yuan
- Liu, Hao
- Hou, Hai-Man
- Shi, Meng-Meng
- Wu, Jun
- Xu, Yu-Ming
Producer: 20171229
In:
Movement disorders : official journal of the Movement Disorder Society vol. 31
Availability: No items available.
|
|
7.
|
Exome sequencing reveals novel SPG11 mutation in hereditary spastic paraplegia with complicated phenotypes. [electronic resource] by
- Li, Yu-sheng
- Mao, Cheng-yuan
- Shi, Chang-he
- Song, Bo
- Wu, Jun
- Qin, Jie
- Ji, Yan
- Niu, Hui-xia
- Luo, Hai-yang
- Shang, Dan-dan
- Sun, Shi-lei
- Xu, Yu-ming
Producer: 20160420
In:
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia vol. 22
Availability: No items available.
|