A mutation in the signal sequence of LRP5 in a family with an osteoporosis-pseudoglioma syndrome (OPPG)-like phenotype indicates a novel disease mechanism for trinucleotide repeats (Q39889751)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A mutation in the signal sequence of LRP5 in a family with an osteoporosis-pseudoglioma syndrome (OPPG)-like phenotype indicates a novel disease mechanism for trinucleotide repeats |
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A mutation in the signal sequence of LRP5 in a family with an osteoporosis-pseudoglioma syndrome (OPPG)-like phenotype indicates a novel disease mechanism for trinucleotide repeats (English)
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Peter Nürnberg
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Bernd Wollnik
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Boi-Dinh Chung
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Minrong Ai
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Jan Freudenberg
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Abdullah Uzümcü
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Oya Uyguner
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Cynthia F Bartels
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Stefan Höning
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Alfredo Ramirez
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Franz-Georg Hanisch
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Matthew L Warman
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Christian Netzer
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1 April 2009
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