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SATB2-associated syndrome caused by a novel SATB2 mutation in a Chinese boy: A case report and literature review
BACKGROUND: Special AT-rich sequence binding protein 2 (SATB2)-associated syndrome (SAS; OMIM 612313) is an autosomal dominant disorder. Alterations in the SATB2 gene have been identified as causative. CASE SUMMARY: We report a case of a 13-year-old Chinese boy with lifelong global developmental del...
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| Veröffentlicht in: | World J Clin Cases |
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| Hauptverfasser: | , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Baishideng Publishing Group Inc
2021
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8316932/ https://ncbi.nlm.nih.gov/pubmed/34368330 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12998/wjcc.v9.i21.6081 |
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