Familial amyloidotic polyneuropathy: a new transthyretin position 30 mutation (alanine for valine) in a family of German descent.
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| Title: | Familial amyloidotic polyneuropathy: a new transthyretin position 30 mutation (alanine for valine) in a family of German descent. |
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| Authors: | Jones LA; Department of Medicine, Boston City Hospital, MA., Skare JC, Cohen AS, Harding JA, Milunsky A, Skinner M |
| Source: | Clinical genetics [Clin Genet] 1992 Feb; Vol. 41 (2), pp. 70-3. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. |
| Journal Info: | Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print Cited Medium: Print ISSN: 0009-9163 (Print) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 1544214 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Familial amyloidotic polyneuropathy: a new transthyretin position 30 mutation (alanine for valine) in a family of German descent. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Jones+LA%22">Jones LA</searchLink>; Department of Medicine, Boston City Hospital, MA.<br /><searchLink fieldCode="AU" term="%22Skare+JC%22">Skare JC</searchLink><br /><searchLink fieldCode="AU" term="%22Cohen+AS%22">Cohen AS</searchLink><br /><searchLink fieldCode="AU" term="%22Harding+JA%22">Harding JA</searchLink><br /><searchLink fieldCode="AU" term="%22Milunsky+A%22">Milunsky A</searchLink><br /><searchLink fieldCode="AU" term="%22Skinner+M%22">Skinner M</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%220253664%22">Clinical genetics</searchLink> [Clin Genet] 1992 Feb; Vol. 41 (2), pp. 70-3. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Munksgaard%22">Munksgaard </searchLink><i>Country of Publication: </i>Denmark <i>NLM ID: </i>0253664 <i>Publication Model: </i>Print <i>Cited Medium: </i>Print <i>ISSN: </i>0009-9163 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200099163%22">00099163 </searchLink><i>NLM ISO Abbreviation: </i>Clin Genet <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=1544214 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1111/j.1399-0004.1992.tb03635.x Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 70 Titles: – TitleFull: Familial amyloidotic polyneuropathy: a new transthyretin position 30 mutation (alanine for valine) in a family of German descent. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Jones LA – PersonEntity: Name: NameFull: Skare JC – PersonEntity: Name: NameFull: Cohen AS – PersonEntity: Name: NameFull: Harding JA – PersonEntity: Name: NameFull: Milunsky A – PersonEntity: Name: NameFull: Skinner M IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 02 Text: 1992 Feb Type: published Y: 1992 Identifiers: – Type: issn-print Value: 0009-9163 Numbering: – Type: volume Value: 41 – Type: issue Value: 2 Titles: – TitleFull: Clinical genetics Type: main |
| ResultId | 1 |