Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene and Review of Literature
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1559-1166
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene and Review of Literature ; volume:72 ; number:11 ; day:17 ; month:10 ; year:2022 ; pages:2242-2251 ; date:11.2022
Journal of molecular neuroscience ; 72, Heft 11 (17.10.2022), 2242-2251, 11.2022
- Creator
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Elaraby, Nesma M.
Ahmed, Hoda A.
Ashaat, Neveen A.
Tawfik, Sameh
Ahmed, Mahmoud K. H.
Hassib, Nehal F.
Ashaat, Engy A.
- Contributor
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SpringerLink (Online service)
- DOI
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10.1007/s12031-022-02074-y
- URN
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urn:nbn:de:101:1-2023021621072502883119
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:53 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Elaraby, Nesma M.
- Ahmed, Hoda A.
- Ashaat, Neveen A.
- Tawfik, Sameh
- Ahmed, Mahmoud K. H.
- Hassib, Nehal F.
- Ashaat, Engy A.
- SpringerLink (Online service)
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A novel variant of DNM1L expanding the clinical phenotypic spectrum: a case report and literature review
Dystonia and Parkinsonism in COA7-related disorders: expanding the phenotypic spectrum
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EIF3F-related neurodevelopmental disorder: refining the phenotypic and expanding the molecular spectrum
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Insights into the expanding intestinal phenotypic spectrum of SOCS1 haploinsufficiency and therapeutic options
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Expanding the phenotypic spectrum of FINCA (fibrosis, neurodegeneration, and cerebral angiomatosis) syndrome beyond infancy
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