ASXL3-related disorder: Molecular phenotyping and comprehensive review providing insights into disease mechanism.
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| Title: | ASXL3-related disorder: Molecular phenotyping and comprehensive review providing insights into disease mechanism. |
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| Authors: | Woods E; Sheffield Clinical Genetics Service, Sheffield Children's Hospital, Sheffield, UK.; Division of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, UK., Holmes N; Sheffield Diagnostic Genetics Service, Sheffield Children's Hospital, Sheffield, UK., Albaba S; Sheffield Diagnostic Genetics Service, Sheffield Children's Hospital, Sheffield, UK., Evans IR; Division of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, UK.; The Bateson Centre, University of Sheffield, Sheffield, UK., Balasubramanian M; Sheffield Clinical Genetics Service, Sheffield Children's Hospital, Sheffield, UK.; Division of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, UK.; The Bateson Centre, University of Sheffield, Sheffield, UK. |
| Source: | Clinical genetics [Clin Genet] 2024 May; Vol. 105 (5), pp. 470-487. Date of Electronic Publication: 2024 Feb 29. |
| Publication Type: | Journal Article; Review |
| Journal Info: | Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| ISSN: | 1399-0004 |
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| DOI: | 10.1111/cge.14506 |
