Cited 7 times in
Glutaric aciduria type 1 in Korea: report of two novel mutations
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 이준수 | - |
dc.date.accessioned | 2019-01-24T16:40:06Z | - |
dc.date.available | 2019-01-24T16:40:06Z | - |
dc.date.issued | 2010 | - |
dc.identifier.issn | 1011-8934 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/166981 | - |
dc.description.abstract | Glutaric aciduria type I (GA I) is an autosomal recessive disorder caused by a deficiency of glutaryl-CoA dehydrogenase. Although over 400 patients confirmed as GA I have been reported, reports from the Asian population had contributed to the minor proportion. We recently diagnosed two cases of GA I confirmed with mutational analysis. Here, we present their rather atypical clinical presentations with genetic characteristics for the first time in Korea. Profound developmental delay from birth, association of hearing loss, and neurological improvement after surgical intervention, were considered to be different clinical features from most reported cases. One patient was a compound heterozygote for p.Ser139Leu and p.Asp220Tyr, and the other for p.Ser139Leu and Glu160X. The mutations of the two alleles (p.Asp220Tyr and p.Glu160X) were novel and reports of p.Ser139Leu were rare both in Western and other Asian populations. These might suggest different genetic spectrum of Korean GA I patients. | - |
dc.description.statementOfResponsibility | open | - |
dc.format | application/pdf | - |
dc.language | English | - |
dc.publisher | 대한의학회(The Korean Academy of Medical Sciences) | - |
dc.relation.isPartOf | JOURNAL OF KOREAN MEDICAL SCIENCE | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.rights | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.subject.MESH | Alleles | - |
dc.subject.MESH | Amino Acid Metabolism, Inborn Errors/genetics* | - |
dc.subject.MESH | Amino Acid Substitution | - |
dc.subject.MESH | Child, Preschool | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Glutaryl-CoA Dehydrogenase/deficiency* | - |
dc.subject.MESH | Glutaryl-CoA Dehydrogenase/genetics* | - |
dc.subject.MESH | Heterozygote | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Infant | - |
dc.subject.MESH | Magnetic Resonance Imaging | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Mutation | - |
dc.subject.MESH | Republic of Korea | - |
dc.subject.MESH | Sequence Analysis, DNA | - |
dc.title | Glutaric aciduria type 1 in Korea: report of two novel mutations | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Pediatrics (소아청소년과학교실) | - |
dc.contributor.googleauthor | June Dong Park | - |
dc.contributor.googleauthor | ByungChan Lim | - |
dc.contributor.googleauthor | Ki Joong Kim | - |
dc.contributor.googleauthor | Yong Seung Hwang | - |
dc.contributor.googleauthor | Seung Ki Kim | - |
dc.contributor.googleauthor | Seong-Ho Kang | - |
dc.contributor.googleauthor | Sung Im Cho | - |
dc.contributor.googleauthor | Sung Sup Park | - |
dc.contributor.googleauthor | Joon Soo Lee | - |
dc.contributor.googleauthor | Jong Hee Chae | - |
dc.identifier.doi | 10.3346/jkms.2010.25.6.957 | - |
dc.contributor.localId | A03177 | - |
dc.relation.journalcode | J01517 | - |
dc.identifier.eissn | 1598-6357 | - |
dc.identifier.pmid | 20514322 | - |
dc.subject.keyword | Glutaric Aciduria Type I | - |
dc.subject.keyword | Glutaryl-CoA Dehydrogenase | - |
dc.subject.keyword | Korea | - |
dc.subject.keyword | Mutation | - |
dc.contributor.alternativeName | Lee, Joon Soo | - |
dc.contributor.affiliatedAuthor | 이준수 | - |
dc.citation.volume | 25 | - |
dc.citation.number | 6 | - |
dc.citation.startPage | 957 | - |
dc.citation.endPage | 960 | - |
dc.identifier.bibliographicCitation | JOURNAL OF KOREAN MEDICAL SCIENCE, Vol.25(6) : 957-960, 2010 | - |
dc.identifier.rimsid | 58369 | - |
dc.type.rims | ART | - |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.