Nelson Chen

Case report: novel PCDH15 variant causes usher syndrome type 1F with congenital hearing loss and syndromic retinitis pigmentosa

Hane Lee, Laura Liu, Nan-Kai Wang, 2022, BMC Ophthalmology.

Congenital Stationary Night Blindness: Clinical and Genetic Features

Hane Lee, Wei-Chi Wu, Laura Liu, 2022, International journal of molecular sciences.

Mouse Models of Achromatopsia in Addressing Temporal “Point of No Return” in Gene-Therapy

S. Tsang, M. Tai, Chyuan-Sheng Lin, 2021, International journal of molecular sciences.

Spatiotemporal control of genome engineering in cone photoreceptors

Chyuan-Sheng Lin, J. Sparrow, Chun‐Wei Hsu, 2023, Cell & Bioscience.

A homozygous in-frame duplication within the LRRCT consensus sequence of CFAP410 causes cone-rod dystrophy, macular staphyloma and short stature

Hane Lee, Wei-Chi Wu, Laura Liu, 2021, Ophthalmic genetics.

Spatiotemporal control of genome engineering in cone photoreceptors

Chyuan-Sheng Lin, J. Sparrow, Chun‐Wei Hsu, 2023, Cell & Bioscience.