Lack of C9orf72 Repeat Expansion in Taiwanese Patients with Mixed Neurodegenerative Disorders

Por Lin, Chin-Hsien, Chen, Ta-Fu, Chiu, Ming-Jang, Lin, Han-I, Wu, Ruey-Meei
Publicado em 2014

A limb-girdle myopathy phenotype of RUNX2 mutation in a patient with cleidocranial dysplasia: a case study and literature review

Por Hsueh, Sung-Ju, Lee, Ni-Chung, Yang, Shu-Hua, Lin, Han-I, Lin, Chin-Hsien
Publicado no BMC Neurol (2017)