Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease.
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| Title: | Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease. |
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| Authors: | Hyeon Jin Kim1, Young Bin Hong1, Jin-Mo Park1, Yu-Ri Choi1, Ye Jin Kim2, Bo Ram Yoon2, Heasoo Koo3, Jeong Hyun Yoo4, Sang Beom Kim5, Minhwa Park6, Ki Wha Chung2 kwchung@kongju.ac.kr, Byung-Ok Choi1 bochoi@ewha.ac.kr |
| Source: | Orphanet Journal of Rare Diseases. 2013, Vol. 8 Issue 1, p1-11. 11p. 1 Black and White Photograph, 4 Charts, 4 Graphs. |
| Database: | Academic Search Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 89708781 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Hyeon+Jin+Kim%22">Hyeon Jin Kim</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Young+Bin+Hong%22">Young Bin Hong</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Jin-Mo+Park%22">Jin-Mo Park</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Yu-Ri+Choi%22">Yu-Ri Choi</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Ye+Jin+Kim%22">Ye Jin Kim</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Bo+Ram+Yoon%22">Bo Ram Yoon</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Heasoo+Koo%22">Heasoo Koo</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Jeong+Hyun+Yoo%22">Jeong Hyun Yoo</searchLink><relatesTo>4</relatesTo><br /><searchLink fieldCode="AR" term="%22Sang+Beom+Kim%22">Sang Beom Kim</searchLink><relatesTo>5</relatesTo><br /><searchLink fieldCode="AR" term="%22Minhwa+Park%22">Minhwa Park</searchLink><relatesTo>6</relatesTo><br /><searchLink fieldCode="AR" term="%22Ki+Wha+Chung%22">Ki Wha Chung</searchLink><relatesTo>2</relatesTo><i> kwchung@kongju.ac.kr</i><br /><searchLink fieldCode="AR" term="%22Byung-Ok+Choi%22">Byung-Ok Choi</searchLink><relatesTo>1</relatesTo><i> bochoi@ewha.ac.kr</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Orphanet+Journal+of+Rare+Diseases%22">Orphanet Journal of Rare Diseases</searchLink>. 2013, Vol. 8 Issue 1, p1-11. 11p. 1 Black and White Photograph, 4 Charts, 4 Graphs. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=89708781 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/1750-1172-8-104 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 11 StartPage: 1 Titles: – TitleFull: Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Hyeon Jin Kim – PersonEntity: Name: NameFull: Young Bin Hong – PersonEntity: Name: NameFull: Jin-Mo Park – PersonEntity: Name: NameFull: Yu-Ri Choi – PersonEntity: Name: NameFull: Ye Jin Kim – PersonEntity: Name: NameFull: Bo Ram Yoon – PersonEntity: Name: NameFull: Heasoo Koo – PersonEntity: Name: NameFull: Jeong Hyun Yoo – PersonEntity: Name: NameFull: Sang Beom Kim – PersonEntity: Name: NameFull: Minhwa Park – PersonEntity: Name: NameFull: Ki Wha Chung – PersonEntity: Name: NameFull: Byung-Ok Choi IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 08 Text: 2013 Type: published Y: 2013 Identifiers: – Type: issn-print Value: 17501172 Numbering: – Type: volume Value: 8 – Type: issue Value: 1 Titles: – TitleFull: Orphanet Journal of Rare Diseases Type: main |
| ResultId | 1 |
