Some DNM2 mutations cause extremely severe congenital myopathy and phenocopy myotubular myopathy.
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| Title: | Some DNM2 mutations cause extremely severe congenital myopathy and phenocopy myotubular myopathy. |
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| Authors: | Biancalana, Valérie1,2,3,4,5 valerie.biancalana@chru-strasbourg.fr, Romero, Norma B.6,7,8, Thuestad, Inger Johanne9, Ignatius, Jaakko10, Kataja, Janne11, Gardberg, Maria12, Héron, Delphine13, Malfatti, Edoardo7,8, Oldfors, Anders14, Laporte, Jocelyn2,3,4,5 |
| Source: | Acta Neuropathologica Communications. 9/12/2018, Vol. 6 Issue 1, pN.PAG-N.PAG. 1p. |
| Database: | Academic Search Ultimate |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 131764361 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Some DNM2 mutations cause extremely severe congenital myopathy and phenocopy myotubular myopathy. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Biancalana%2C+Valérie%22">Biancalana, Valérie</searchLink><relatesTo>1,2,3,4,5</relatesTo><i> valerie.biancalana@chru-strasbourg.fr</i><br /><searchLink fieldCode="AR" term="%22Romero%2C+Norma+B%2E%22">Romero, Norma B.</searchLink><relatesTo>6,7,8</relatesTo><br /><searchLink fieldCode="AR" term="%22Thuestad%2C+Inger+Johanne%22">Thuestad, Inger Johanne</searchLink><relatesTo>9</relatesTo><br /><searchLink fieldCode="AR" term="%22Ignatius%2C+Jaakko%22">Ignatius, Jaakko</searchLink><relatesTo>10</relatesTo><br /><searchLink fieldCode="AR" term="%22Kataja%2C+Janne%22">Kataja, Janne</searchLink><relatesTo>11</relatesTo><br /><searchLink fieldCode="AR" term="%22Gardberg%2C+Maria%22">Gardberg, Maria</searchLink><relatesTo>12</relatesTo><br /><searchLink fieldCode="AR" term="%22Héron%2C+Delphine%22">Héron, Delphine</searchLink><relatesTo>13</relatesTo><br /><searchLink fieldCode="AR" term="%22Malfatti%2C+Edoardo%22">Malfatti, Edoardo</searchLink><relatesTo>7,8</relatesTo><br /><searchLink fieldCode="AR" term="%22Oldfors%2C+Anders%22">Oldfors, Anders</searchLink><relatesTo>14</relatesTo><br /><searchLink fieldCode="AR" term="%22Laporte%2C+Jocelyn%22">Laporte, Jocelyn</searchLink><relatesTo>2,3,4,5</relatesTo> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Acta+Neuropathologica+Communications%22">Acta Neuropathologica Communications</searchLink>. 9/12/2018, Vol. 6 Issue 1, pN.PAG-N.PAG. 1p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=131764361 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s40478-018-0593-2 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 1 StartPage: N.PAG Titles: – TitleFull: Some DNM2 mutations cause extremely severe congenital myopathy and phenocopy myotubular myopathy. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Biancalana, Valérie – PersonEntity: Name: NameFull: Romero, Norma B. – PersonEntity: Name: NameFull: Thuestad, Inger Johanne – PersonEntity: Name: NameFull: Ignatius, Jaakko – PersonEntity: Name: NameFull: Kataja, Janne – PersonEntity: Name: NameFull: Gardberg, Maria – PersonEntity: Name: NameFull: Héron, Delphine – PersonEntity: Name: NameFull: Malfatti, Edoardo – PersonEntity: Name: NameFull: Oldfors, Anders – PersonEntity: Name: NameFull: Laporte, Jocelyn IsPartOfRelationships: – BibEntity: Dates: – D: 12 M: 09 Text: 9/12/2018 Type: published Y: 2018 Identifiers: – Type: issn-print Value: 20515960 Numbering: – Type: volume Value: 6 – Type: issue Value: 1 Titles: – TitleFull: Acta Neuropathologica Communications Type: main |
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