Biallelic Truncating DNAH14 Variant in Siblings with Neurodevelopmental Disorder and Predominant Ataxia: Clinical Report and Literature Review.
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| Title: | Biallelic Truncating DNAH14 Variant in Siblings with Neurodevelopmental Disorder and Predominant Ataxia: Clinical Report and Literature Review. |
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| Authors: | Baris, Savas1 (AUTHOR), Dogan, Mustafa2 (AUTHOR) mustafadogan@gelisimlab.com.tr, Terali, Kerem3 (AUTHOR), Gezdirici, Alper4 (AUTHOR), Eroz, Recep5 (AUTHOR), Yucel, Peren Perk6 (AUTHOR), Kilic, Huseyin7 (AUTHOR), Yavas, Cuneyd8 (AUTHOR), Yildirim, Gizem4,9 (AUTHOR), Baris, Ibrahim1,9 (AUTHOR) |
| Source: | International Journal of Molecular Sciences. Jan2026, Vol. 27 Issue 2, p575. 15p. |
| 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: 191172894 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Biallelic Truncating DNAH14 Variant in Siblings with Neurodevelopmental Disorder and Predominant Ataxia: Clinical Report and Literature Review. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Baris%2C+Savas%22">Baris, Savas</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Dogan%2C+Mustafa%22">Dogan, Mustafa</searchLink><relatesTo>2</relatesTo> (AUTHOR)<i> mustafadogan@gelisimlab.com.tr</i><br /><searchLink fieldCode="AR" term="%22Terali%2C+Kerem%22">Terali, Kerem</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Gezdirici%2C+Alper%22">Gezdirici, Alper</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Eroz%2C+Recep%22">Eroz, Recep</searchLink><relatesTo>5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Yucel%2C+Peren+Perk%22">Yucel, Peren Perk</searchLink><relatesTo>6</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Kilic%2C+Huseyin%22">Kilic, Huseyin</searchLink><relatesTo>7</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Yavas%2C+Cuneyd%22">Yavas, Cuneyd</searchLink><relatesTo>8</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Yildirim%2C+Gizem%22">Yildirim, Gizem</searchLink><relatesTo>4,9</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Baris%2C+Ibrahim%22">Baris, Ibrahim</searchLink><relatesTo>1,9</relatesTo> (AUTHOR) – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22International+Journal+of+Molecular+Sciences%22">International Journal of Molecular Sciences</searchLink>. Jan2026, Vol. 27 Issue 2, p575. 15p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=191172894 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.3390/ijms27020575 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 15 StartPage: 575 Titles: – TitleFull: Biallelic Truncating DNAH14 Variant in Siblings with Neurodevelopmental Disorder and Predominant Ataxia: Clinical Report and Literature Review. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Baris, Savas – PersonEntity: Name: NameFull: Dogan, Mustafa – PersonEntity: Name: NameFull: Terali, Kerem – PersonEntity: Name: NameFull: Gezdirici, Alper – PersonEntity: Name: NameFull: Eroz, Recep – PersonEntity: Name: NameFull: Yucel, Peren Perk – PersonEntity: Name: NameFull: Kilic, Huseyin – PersonEntity: Name: NameFull: Yavas, Cuneyd – PersonEntity: Name: NameFull: Yildirim, Gizem – PersonEntity: Name: NameFull: Baris, Ibrahim IsPartOfRelationships: – BibEntity: Dates: – D: 15 M: 01 Text: Jan2026 Type: published Y: 2026 Identifiers: – Type: issn-print Value: 16616596 Numbering: – Type: volume Value: 27 – Type: issue Value: 2 Titles: – TitleFull: International Journal of Molecular Sciences Type: main |
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