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
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| Main Authors: | , , |
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| Format: | Article (Journal) |
| Language: | English |
| Published: |
1 August 2016
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| In: |
Endocrine reviews
Year: 2016, Volume: 37, Issue: 4, Pages: 417-448 |
| ISSN: | 1945-7189 |
| DOI: | 10.1210/er.2016-1036 |
| Online Access: | 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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| Author Notes: | Antonio Marchini, Tsutomu Ogata, and Gudrun A. Rappold |
| Summary: | Abstract. SHOX deficiency is the most frequent genetic growth disorder associated with isolated and syndromic forms of short stature. Caused by mutations in th |
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| Item Description: | Gesehen am 08.11.2018 |
| Physical Description: | Online Resource |
| ISSN: | 1945-7189 |
| DOI: | 10.1210/er.2016-1036 |