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Barth Syndrome Is Associated with a Cognitive Phenotype
OBJECTIVE: Barth syndrome is a rare, X-linked recessive disorder that affects only boys. The cardinal characteristics include growth retardation, cardioskeletal myopathy, chronic or cyclic neutropenia, and 3-methylglutaconic aciduria. A preliminary study of five young boys with Barth syndrome sugges...
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| Autors principals: | , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2007
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2813702/ https://ncbi.nlm.nih.gov/pubmed/17353728 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/01.DBP.0000257519.79803.90 |
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