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1. Assessment of GGC Repeat Expansion in GIPC1 in Patients with Parkinson's Disease. Issue 7 (6th May 2022)

2. Association of rare variants in neurodegenerative genes with familial Alzheimer's disease. Issue 10 (17th September 2020)

4. Clinical features and reclassification of essential tremor with NOTCH2NLC GGC repeat expansions based on a long‐term follow‐up. (25th September 2022)

5. Clinical features of NOTCH2NLC-related neuronal intranuclear inclusion disease. Issue 12 (23rd September 2022)

7. Familial amyloid polyneuropathy with chronic paroxysmal dry cough in Mainland China: A Chinese family with a proven heterozygous missense mutation c.349G>T in the transthyretin gene. (February 2019)

10. Homozygosity mapping and next generation sequencing for the genetic diagnosis of hereditary ataxia and spastic paraplegia in consanguineous families. (November 2020)