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)
Jump to navigation
Jump to search
scientific article
| 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 |
scientific article |
Statements
1 reference
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)
1 reference
Peter Nürnberg
1 reference
Bernd Wollnik
1 reference
Boi-Dinh Chung
1 reference
Minrong Ai
1 reference
Jan Freudenberg
1 reference
Abdullah Uzümcü
1 reference
Oya Uyguner
1 reference
Cynthia F Bartels
1 reference
Stefan Höning
1 reference
Alfredo Ramirez
1 reference
Franz-Georg Hanisch
1 reference
Matthew L Warman
1 reference
Christian Netzer
1 reference
1 April 2009
1 reference
1 reference
30
1 reference
4
1 reference
641-648
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
Identifiers
1 reference
1 reference