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1. A Novel SPAST Mutation Results in Spastin Accumulation and Defects in Microtubule Dynamics. Issue 3 (20th December 2021)

2. A PRRT2 variant in a Chinese family with paroxysmal kinesigenic dyskinesia and benign familial infantile seizures results in loss of interaction with STX1B. (15th July 2018)

8. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1. Issue 1 (2nd January 2021)

9. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1. Issue 1 (2nd January 2021)