Exome Sequencing Identifies a c.148-1G>C Mutation of TBX5 in a Holt-Oram Family with Unusual Genotype-Phenotype Correlations
Background/Aims: Congenital heart defects (CHD) can occur with upper limbs deformities. Holt-Oram syndrome is the main type of heart-hand syndromes, characterized by upper limb radial ray malformations, CHD and/or conduction abnormalities. Mutations of the TBX5 gene, most of which are found within t...
محفوظ في:
| المؤلفون الرئيسيون: | , , , , , |
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| التنسيق: | Artigo |
| اللغة: | Inglês |
| منشور في: |
Cell Physiol Biochem Press GmbH & Co KG
2015-09-01
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| سلاسل: | Cellular Physiology and Biochemistry |
| الموضوعات: | |
| الوصول للمادة أونلاين: | http://www.karger.com/Article/FullText/430232 |
| الوسوم: |
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