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Exons deletion of CNKSR2 gene identified in X-linked syndromic intellectual disability
BACKGROUND: The Houge type of X-linked syndromic mental retardation is an X-linked intellectual disability (XLID) recently recorded in the Online Mendelian Inheritance in Man (OMIM) and only 8 cases have been reported in literature thus far. CASE PRESENTATION: We present two brothers with intractabl...
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| izdano v: | BMC Med Genet |
|---|---|
| Main Authors: | , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
BioMed Central
2020
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7119275/ https://ncbi.nlm.nih.gov/pubmed/32245427 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-020-01004-2 |
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