Format

Send to

Choose Destination
J Neurol Sci. 2017 Nov 15;382:166-167. doi: 10.1016/j.jns.2017.09.046. Epub 2017 Sep 30.

Author reply: "MtDNA m.3472T>C could be classified as a primary mutation of Leber's hereditary optic neuropathy".

Author information

1
Department of Laboratory Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Republic of Korea.
2
Department of Laboratory Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Republic of Korea; Biomedical Research Institute, Seoul National University Hospital, Seoul, Republic of Korea.
3
Biomedical Research Institute, Seoul National University Hospital, Seoul, Republic of Korea. Electronic address: jkimmd@snu.ac.kr.
4
Department of Ophthalmology, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam, Republic of Korea. Electronic address: hjm@snu.ac.kr.
PMID:
28992946
DOI:
10.1016/j.jns.2017.09.046
[Indexed for MEDLINE]

Supplemental Content

Full text links

Icon for Elsevier Science
Loading ...
Support Center