Recurrent mutations in the deafness gene GJB2 (connexin 26) in British Asian families.
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| Title: | Recurrent mutations in the deafness gene GJB2 (connexin 26) in British Asian families. |
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| Authors: | Rickard S, Kelsell DP, Sirimana T, Rajput K, MacArdle B, Bitner-Glindzicz M |
| Source: | Journal of medical genetics [J Med Genet] 2001 Aug; Vol. 38 (8), pp. 530-3. |
| Publication Type: | Letter; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Print Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 11494963 AccessLevel: 2 PubType: Report PubTypeId: report PreciseRelevancyScore: 0 |
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| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=11494963 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1136/jmg.38.8.530 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 530 Titles: – TitleFull: Recurrent mutations in the deafness gene GJB2 (connexin 26) in British Asian families. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Rickard S – PersonEntity: Name: NameFull: Kelsell DP – PersonEntity: Name: NameFull: Sirimana T – PersonEntity: Name: NameFull: Rajput K – PersonEntity: Name: NameFull: MacArdle B – PersonEntity: Name: NameFull: Bitner-Glindzicz M IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 08 Text: 2001 Aug Type: published Y: 2001 Identifiers: – Type: issn-electronic Value: 1468-6244 Numbering: – Type: volume Value: 38 – Type: issue Value: 8 Titles: – TitleFull: Journal of medical genetics Type: main |
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