14 results on '"Guo, Xia‐Nan"'
Search Results
2. Positive association of serum FUT8 activity with renal tubulointerstitial injury in IgA nephropathy patients
3. Identification of a novel loss-of-function C9orf72 splice site mutation in a patient with amyotrophic lateral sclerosis
4. TMEM151AVariants Cause Paroxysmal Kinesigenic Dyskinesia: A Large‐Sample Study
5. Re-evaluation of PRRT2 mutations in paroxysmal disorders
6. The Phenotypic and Genetic Spectrum of Paroxysmal Kinesigenic Dyskinesia in China
7. TMEM151A Variants Cause Paroxysmal Kinesigenic Dyskinesia: A Large‐Sample Study.
8. A proposed synergistic effect of CSF1R and NMUR2 variants contributes to binge eating in hereditary diffuse leukoencephalopathy with spheroids
9. Whole-exome sequencing identifies a missense mutation in hnRNPA1 in a family with flail arm ALS
10. Mutation spectrum of Chinese patients with familial and sporadic amyotrophic lateral sclerosis
11. Quick Genetic Screening Using Targeted Next-Generation Sequencing in Patients With Tuberous Sclerosis
12. Quick Genetic Screening Using Targeted Next-Generation Sequencing in Patients With Tuberous Sclerosis.
13. Whole-exome sequencing identifies a missense mutation in hnRNPA1in a family with flail arm ALS
14. Mutation spectrum of Chinese patients with familial and sporadic amyotrophic lateral sclerosis.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.