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De novo mutations in ARID1B associated with both syndromic and non-syndromic short stature
BACKGROUND: Human height is a complex trait with a strong genetic basis. Recently, a significant association between rare copy number variations (CNVs) and short stature has been identified, and candidate genes in these rare CNVs are being explored. This study aims to evaluate the association betwee...
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| Publicado no: | BMC Genomics |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4574214/ https://ncbi.nlm.nih.gov/pubmed/26376624 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-015-1898-1 |
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