ARL6IP1 mutation causes congenital insensitivity to pain, acromutilation and spastic paraplegia.
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| Title: | ARL6IP1 mutation causes congenital insensitivity to pain, acromutilation and spastic paraplegia. |
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| Authors: | Nizon, M.1, Küry, S.1, Péréon, Y.2, Besnard, T.1, Quinquis, D.1, Boisseau, P.1, Marsaud, T.1, Magot, A.2, Mussini, J.‐M.3, Mayrargue, E.4, Barbarot, S.5, Bézieau, S.1, Isidor, B.1 bertrand.isidor@chu-nantes.fr |
| Source: | Clinical Genetics. Jan2018, Vol. 93 Issue 1, p169-172. 4p. 1 Color Photograph, 1 Graph. |
| Database: | Academic Search Ultimate |
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| FullText | Links: – Type: pdflink Text: Availability: 1 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 126849918 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=126849918 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1111/cge.13048 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 4 StartPage: 169 Titles: – TitleFull: ARL6IP1 mutation causes congenital insensitivity to pain, acromutilation and spastic paraplegia. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Nizon, M. – PersonEntity: Name: NameFull: Küry, S. – PersonEntity: Name: NameFull: Péréon, Y. – PersonEntity: Name: NameFull: Besnard, T. – PersonEntity: Name: NameFull: Quinquis, D. – PersonEntity: Name: NameFull: Boisseau, P. – PersonEntity: Name: NameFull: Marsaud, T. – PersonEntity: Name: NameFull: Magot, A. – PersonEntity: Name: NameFull: Mussini, J.‐M. – PersonEntity: Name: NameFull: Mayrargue, E. – PersonEntity: Name: NameFull: Barbarot, S. – PersonEntity: Name: NameFull: Bézieau, S. – PersonEntity: Name: NameFull: Isidor, B. IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 01 Text: Jan2018 Type: published Y: 2018 Identifiers: – Type: issn-print Value: 00099163 Numbering: – Type: volume Value: 93 – Type: issue Value: 1 Titles: – TitleFull: Clinical Genetics Type: main |
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