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A novel double mutation in cis in MFN2 causes Charcot-Marie-Tooth neuropathy type 2A
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Park, Su-Yeon | - |
dc.contributor.author | Kim, So Yeon | - |
dc.contributor.author | Hong, Yoon-Ho | - |
dc.contributor.author | Cho, Sung Im | - |
dc.contributor.author | Seong, Moon-Woo | - |
dc.contributor.author | Park, Sung Sup | - |
dc.creator | 홍윤호 | - |
dc.date.accessioned | 2013-03-22T02:52:11Z | - |
dc.date.available | 2013-03-22T02:52:11Z | - |
dc.date.issued | 2012-08 | - |
dc.identifier.citation | NEUROGENETICS Vol.13 No.3, pp. 275-280 | - |
dc.identifier.issn | 1364-6745 | - |
dc.identifier.uri | https://hdl.handle.net/10371/81404 | - |
dc.description.abstract | Mutations in mitofusin-2 (MFN2) are the most common cause of axonal Charcot-Marie-Tooth (CMT) neuropathy. Herein, we report a novel double mutation in cis (c.[474+4A > G; 668T > A]) in a Korean family with late-onset autosomal dominant mild axonal CMT. Transcriptional analysis demonstrated aberrant splicing with exon 5 skipping and premature termination of translation before the missense mutation in exon 7. Interestingly, the aberrant splicing was incomplete, with some of the primary transcripts being spliced correctly and expressing the downstream missense mutation. The pathogenic relevance of the missense mutation would not be appreciated without the leaky aberrant splicing and the insensitivity of MFN2 to haploinsufficiency. | en |
dc.language.iso | en | en |
dc.publisher | SPRINGER | en |
dc.subject | 복합학 | en |
dc.subject | MFN2 | - |
dc.subject | Charcot–Marie–Tooth neuropathy | - |
dc.subject | Double mutation in cis | - |
dc.subject | Korean | - |
dc.title | A novel double mutation in cis in MFN2 causes Charcot-Marie-Tooth neuropathy type 2A | en |
dc.type | Article | - |
dc.contributor.AlternativeAuthor | 박수연 | - |
dc.contributor.AlternativeAuthor | 김소연 | - |
dc.contributor.AlternativeAuthor | 홍윤호 | - |
dc.contributor.AlternativeAuthor | 조성임 | - |
dc.contributor.AlternativeAuthor | 성문우 | - |
dc.contributor.AlternativeAuthor | 박성섭 | - |
dc.identifier.doi | 10.1007/s10048-012-0327-8 | - |
dc.description.srnd | OAIID:oai:osos.snu.ac.kr:snu2012-01/102/2008000967/1 | - |
dc.description.srnd | SEQ:1 | - |
dc.description.srnd | PERF_CD:SNU2012-01 | - |
dc.description.srnd | EVAL_ITEM_CD:102 | - |
dc.description.srnd | USER_ID:2008000967 | - |
dc.description.srnd | ADJUST_YN:Y | - |
dc.description.srnd | EMP_ID:A077101 | - |
dc.description.srnd | DEPT_CD:801 | - |
dc.description.srnd | CITE_RATE:3.354 | - |
dc.description.srnd | FILENAME:MFN2_neurogenetics.pdf | - |
dc.description.srnd | DEPT_NM:의학과 | - |
dc.description.srnd | EMAIL:yhh@snu.ac.kr | - |
dc.description.srnd | SCOPUS_YN:Y | - |
dc.description.srnd | CONFIRM:Y | - |
dc.identifier.srnd | 2012-01/102/2008000967/1 | - |
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