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Identification of Novel SHOX Target Genes in the Developing Limb Using a Transgenic Mouse Model
Deficiency of the human short stature homeobox-containing gene (SHOX) has been identified in several disorders characterized by reduced height and skeletal anomalies such as Turner syndrome, Léri-Weill dyschondrosteosis and Langer mesomelic dysplasia as well as isolated short stature. SHOX acts as a...
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| 主要な著者: | , , , , , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Public Library of Science
2014
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4041798/ https://ncbi.nlm.nih.gov/pubmed/24887312 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0098543 |
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