Anni Zhu

A homozygous SLITRK6 nonsense mutation is associated with progressive auditory neuropathy in humans

E. Puffenberger, K. Strauss, R. O'reilly, 2014, The Laryngoscope.

CODAS syndrome is associated with mutations of LONP1, encoding mitochondrial AAA+ Lon protease.

E. Puffenberger, K. Strauss, S. Sarafianos, 2015, American journal of human genetics.

Ginsenoside Rh4 delays skeletal muscle aging through SIRT1 pathway.

Daidi Fan, Zhiguang Duan, C. Zhu, 2023, Phytomedicine : international journal of phytotherapy and phytopharmacology.

A homozygous SLITRK6 nonsense mutation is associated with progressive auditory neuropathy in humans

E. Puffenberger, K. Strauss, R. O'reilly, 2014, The Laryngoscope.