A track record on SHOX: from basic research to complex models and therapy
Abstract. SHOX deficiency is the most frequent genetic growth disorder associated with isolated and syndromic forms of short stature. Caused by mutations in th
Gespeichert in:
| Hauptverfasser: | , , |
|---|---|
| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
1 August 2016
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| In: |
Endocrine reviews
Year: 2016, Jahrgang: 37, Heft: 4, Pages: 417-448 |
| ISSN: | 1945-7189 |
| DOI: | 10.1210/er.2016-1036 |
| Online-Zugang: | Verlag, Volltext: http://dx.doi.org/10.1210/er.2016-1036 Verlag, Volltext: https://academic.oup.com/edrv/article/37/4/417/2567101 
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| Verfasserangaben: | Antonio Marchini, Tsutomu Ogata, and Gudrun A. Rappold |
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