A novel point mutation A170P in the SHOX gene defines impaired nuclear translocation as a molecular cause for Léri-Weill dyschondrosteosis and Langer dysplasia (Q35446094)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A novel point mutation A170P in the SHOX gene defines impaired nuclear translocation as a molecular cause for Léri-Weill dyschondrosteosis and Langer dysplasia |
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A novel point mutation A170P in the SHOX gene defines impaired nuclear translocation as a molecular cause for Léri-Weill dyschondrosteosis and Langer dysplasia (English)
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Sabherwal N
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Blaschke RJ
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Marchini A
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Heine-Suner D
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Rosell J
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Ferragut J
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Blum WF
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Rappold G
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1 June 2004
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41
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6
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e83
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