Analysis of clinical manifestations and genetic mutations in a child with Laron syndrome
OBJECTIVE: To analyze clinical manifestations and gene mutations in a child with severe short stature, explore its molecular mechanism and further clarify the diagnostic procedure for short stature
| Veröffentlicht in: | Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 51(2013), 12 vom: 03. Dez., Seite 930-3 |
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| 1. Verfasser: | |
| Weitere Verfasser: | , , , |
| Format: | Aufsatz |
| Sprache: | Chinese |
| Veröffentlicht: |
2013
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| Zugriff auf das übergeordnete Werk: | Zhonghua er ke za zhi = Chinese journal of pediatrics |
| Schlagworte: | Case Reports English Abstract Journal Article Research Support, Non-U.S. Gov't Insulin-Like Growth Factor Binding Protein 3 Receptors, Somatotropin STAT5 Transcription Factor STAT5B protein, human Human Growth Hormone 12629-01-5 mehr... |