Compound mitochondrial DNA mutations in a neurological patient with ataxia, myoclonus and deafness

Ji Hoon Park, Bo Ram Yoon, Hye Jin Kim, philhyu Lee, Byung Ok Choi, Ki Wha Chung

Research output: Contribution to journalArticle

2 Citations (Scopus)
Original languageEnglish
Pages (from-to)173-177
Number of pages5
JournalJournal of Genetics
Volume93
Issue number1
DOIs
Publication statusPublished - 2014 Jan 1

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DNA Mutational Analysis
Myoclonus
Polyneuropathies
Deafness
Ataxia
Pedigree
Mitochondrial DNA
Case-Control Studies
Mutation
Hunt's syndrome

All Science Journal Classification (ASJC) codes

  • Genetics

Cite this

Park, Ji Hoon ; Yoon, Bo Ram ; Kim, Hye Jin ; Lee, philhyu ; Choi, Byung Ok ; Chung, Ki Wha. / Compound mitochondrial DNA mutations in a neurological patient with ataxia, myoclonus and deafness. In: Journal of Genetics. 2014 ; Vol. 93, No. 1. pp. 173-177.
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Compound mitochondrial DNA mutations in a neurological patient with ataxia, myoclonus and deafness. / Park, Ji Hoon; Yoon, Bo Ram; Kim, Hye Jin; Lee, philhyu; Choi, Byung Ok; Chung, Ki Wha.

In: Journal of Genetics, Vol. 93, No. 1, 01.01.2014, p. 173-177.

Research output: Contribution to journalArticle

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AU - Choi, Byung Ok

AU - Chung, Ki Wha

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