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Ann Clin Lab Sci. 2018 Jul;48(4):546-548.

Neuropathy, Ataxia, Retinitis Pigmentosa-like Phenotype Associated with a Mitochondrial G8363A Mutation in a Family.

Author information

1
Department of Pediatrics, Pediatric Neuroscience Center, Seoul National University Children's Hospital.
2
Department of Pediatrics, College of Medicine, Catholic University of Korea.
3
Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, Korea.
4
Department of Pediatrics, College of Medicine, Catholic University of Korea iglee@catholic.ac.kr chaeped1@snu.ac.kr.
PMID:
30143501
[Indexed for MEDLINE]

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