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New AP4B1 mutation in an African-American child associated with intellectual disability
Prevalence of intellectual disability (ID) varies from 1–3%. Genetic causes of ID are being increasingly recognized. Although multiple mutations have been identified as a cause of syndromic ID, the genetic etiology of non-syndromic ID is poorly understood. However, more than 100 loci have been mappe...
Enregistré dans:
| Publié dans: | J Pediatr Genet |
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| Auteur principal: | |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Georg Thieme Verlag KG
2013
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5020979/ https://ncbi.nlm.nih.gov/pubmed/27625858 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/PGE-13068 |
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