Familial hyperproinsulinaemia due to a mutation substituting histidine for arginine at position 65 in proinsulin: identification of the mutation by restriction enzyme mapping.
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| Title: | Familial hyperproinsulinaemia due to a mutation substituting histidine for arginine at position 65 in proinsulin: identification of the mutation by restriction enzyme mapping. |
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| Authors: | Collinet, M., Berthelon, M., Bénit, P., Laborde, K., Desbuquois, B., Munnich, A., Robert, J. J., Bénit, P (AUTHOR) |
| Source: | European Journal of Pediatrics. 1998, Vol. 157 Issue 6, p456-460. 5p. |
| Database: | Academic Search Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 4681397 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Familial hyperproinsulinaemia due to a mutation substituting histidine for arginine at position 65 in proinsulin: identification of the mutation by restriction enzyme mapping. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Collinet%2C+M%2E%22">Collinet, M.</searchLink><br /><searchLink fieldCode="AR" term="%22Berthelon%2C+M%2E%22">Berthelon, M.</searchLink><br /><searchLink fieldCode="AR" term="%22Bénit%2C+P%2E%22">Bénit, P.</searchLink><br /><searchLink fieldCode="AR" term="%22Laborde%2C+K%2E%22">Laborde, K.</searchLink><br /><searchLink fieldCode="AR" term="%22Desbuquois%2C+B%2E%22">Desbuquois, B.</searchLink><br /><searchLink fieldCode="AR" term="%22Munnich%2C+A%2E%22">Munnich, A.</searchLink><br /><searchLink fieldCode="AR" term="%22Robert%2C+J%2E+J%2E%22">Robert, J. J.</searchLink><br /><searchLink fieldCode="AR" term="%22Bénit%2C+P%22">Bénit, P</searchLink> (AUTHOR) – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22European+Journal+of+Pediatrics%22">European Journal of Pediatrics</searchLink>. 1998, Vol. 157 Issue 6, p456-460. 5p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=4681397 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1007/s004310050852 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 5 StartPage: 456 Titles: – TitleFull: Familial hyperproinsulinaemia due to a mutation substituting histidine for arginine at position 65 in proinsulin: identification of the mutation by restriction enzyme mapping. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Collinet, M. – PersonEntity: Name: NameFull: Berthelon, M. – PersonEntity: Name: NameFull: Bénit, P. – PersonEntity: Name: NameFull: Laborde, K. – PersonEntity: Name: NameFull: Desbuquois, B. – PersonEntity: Name: NameFull: Munnich, A. – PersonEntity: Name: NameFull: Robert, J. J. – PersonEntity: Name: NameFull: Bénit, P IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 06 Text: 1998 Type: published Y: 1998 Identifiers: – Type: issn-print Value: 03406199 Numbering: – Type: volume Value: 157 – Type: issue Value: 6 Titles: – TitleFull: European Journal of Pediatrics Type: main |
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