Author/Creator: Lin, Han-I - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Lin, Han-I

1. A limb-girdle myopathy phenotype of RUNX2 mutation in a patient with cleidocranial dysplasia: a case study and literature review. Issue 1 (December 2017)

Authors:: Hsueh, Sung-Ju; Lee, Ni-Chung; Yang, Shu-Hua; Lin, Han-I; Lin, Chin-Hsien
Journal:: BMC neurology
Issue:: Volume 17:Issue 1(2017)
Page Start:: 1
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

2. A novel C19orf12 frameshift mutation in a MPAN pedigree impairs mitochondrial function and connectivity leading to neurodegeneration. (April 2023)

Authors:: Chen, Huan-Yun; Lin, Han-I; Hsu, Chia-Lang; Chen, Pei-Lung; Huang, Cheng-Yen; Teng, Shu-Chun; Lin, Chin-Hsien
Journal:: Parkinsonism & related disorders
Issue:: Volume 109(2023)
Page Start:
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

3. Genetic analysis of IMPDH2 gene in Taiwanese patients with isolated or combined dystonia. (February 2023)

Authors:: Chen, Pin-Shiuan; Wu, Meng-Chen; Tai, Chun-Hwei; Chang, Yung-Yee; Lan, Min-Yu; Chen, Ying-Fa; Lin, Han-I; Lee, Ni-Chung; Lin, Chin-Hsien
Journal:: Parkinsonism & related disorders
Issue:: Volume 107(2023)
Page Start:
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗