A novel mutation af Cln3 associated with delayed-classic juvenile ceroid lipofuscinois and autophagic vacuolar myopathy.
Saved in:
| Title: | A novel mutation af Cln3 associated with delayed-classic juvenile ceroid lipofuscinois and autophagic vacuolar myopathy. |
|---|---|
| Authors: | Licchetta, L.1,2 laura.licchetta2@unibo.it, Bisulli, F.1,2, Fietz, M.3, Valentino, M.L.1,2, Morbin, M.4, Mostacci, B.1, Oliver, K.L.5, Berkovic, S.F.5, Tinuper, P.1,2 |
| Source: | European Journal of Medical Genetics. Oct2015, Vol. 58 Issue 10, p540-544. 5p. |
| Database: | Academic Search Ultimate |
| FullText | Text: Availability: 0 |
|---|---|
| Header | DbId: asn DbLabel: Academic Search Ultimate An: 110656796 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
| IllustrationInfo | |
| Items | – Name: Title Label: Title Group: Ti Data: A novel mutation af Cln3 associated with delayed-classic juvenile ceroid lipofuscinois and autophagic vacuolar myopathy. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Licchetta%2C+L%2E%22">Licchetta, L.</searchLink><relatesTo>1,2</relatesTo><i> laura.licchetta2@unibo.it</i><br /><searchLink fieldCode="AR" term="%22Bisulli%2C+F%2E%22">Bisulli, F.</searchLink><relatesTo>1,2</relatesTo><br /><searchLink fieldCode="AR" term="%22Fietz%2C+M%2E%22">Fietz, M.</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Valentino%2C+M%2EL%2E%22">Valentino, M.L.</searchLink><relatesTo>1,2</relatesTo><br /><searchLink fieldCode="AR" term="%22Morbin%2C+M%2E%22">Morbin, M.</searchLink><relatesTo>4</relatesTo><br /><searchLink fieldCode="AR" term="%22Mostacci%2C+B%2E%22">Mostacci, B.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Oliver%2C+K%2EL%2E%22">Oliver, K.L.</searchLink><relatesTo>5</relatesTo><br /><searchLink fieldCode="AR" term="%22Berkovic%2C+S%2EF%2E%22">Berkovic, S.F.</searchLink><relatesTo>5</relatesTo><br /><searchLink fieldCode="AR" term="%22Tinuper%2C+P%2E%22">Tinuper, P.</searchLink><relatesTo>1,2</relatesTo> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22European+Journal+of+Medical+Genetics%22">European Journal of Medical Genetics</searchLink>. Oct2015, Vol. 58 Issue 10, p540-544. 5p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=110656796 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1016/j.ejmg.2015.09.002 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 5 StartPage: 540 Titles: – TitleFull: A novel mutation af Cln3 associated with delayed-classic juvenile ceroid lipofuscinois and autophagic vacuolar myopathy. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Licchetta, L. – PersonEntity: Name: NameFull: Bisulli, F. – PersonEntity: Name: NameFull: Fietz, M. – PersonEntity: Name: NameFull: Valentino, M.L. – PersonEntity: Name: NameFull: Morbin, M. – PersonEntity: Name: NameFull: Mostacci, B. – PersonEntity: Name: NameFull: Oliver, K.L. – PersonEntity: Name: NameFull: Berkovic, S.F. – PersonEntity: Name: NameFull: Tinuper, P. IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 10 Text: Oct2015 Type: published Y: 2015 Identifiers: – Type: issn-print Value: 17697212 Numbering: – Type: volume Value: 58 – Type: issue Value: 10 Titles: – TitleFull: European Journal of Medical Genetics Type: main |
| ResultId | 1 |