K. Yu

A novel mitofusin 2 gene mutation causing Charcot-Marie-Tooth type 2A disease in a Chinese family.

C. Ching, Y. Chan, K. Lau, 2010, Chinese medical journal.

[Clinical and genetic analysis of a family with Joubert syndrome type 10 caused by OFD1 gene mutation].

H. Zhang, Y. Liu, W. Li, 2017, Zhonghua er ke za zhi = Chinese journal of pediatrics.

Clinical and Genetic Characterization of Huntington Disease among Hong Kong Chinese – A 5-year Review

K. Au, W. Poon, C. Mak, 2018 .