Published in
Wiley, Human Mutation: Variation, Informatics and Disease, 4(30), p. 641-648, 2009
DOI: 10.1002/humu.20916
Links
Tools
A mutation in the signal sequence ofLRP5in a family with an osteoporosis-pseudoglioma syndrome (OPPG)-like phenotype indicates a novel disease mechanism for trinucleotide repeats
Journal article published in 2009 by
Boi-Dinh Chung,
Hülya Kayserili,
Minrong Ai,
Jan Freudenberg,
Abdullah Üzümcü,
Oya Uyguner,
Cynthia F. Bartels,
Stefan Höning,
Alfredo Ramirez 
,
Franz-Georg Hanisch,
Gudrun Nürnberg,
Peter Nürnberg,
Matthew L. Warman,
Bernd Wollnik,
Christian Kubisch
and other authors.
,
Franz-Georg Hanisch,
Gudrun Nürnberg,
Peter Nürnberg,
Matthew L. Warman,
Bernd Wollnik,
Christian Kubisch
and other authors.
This paper was not found in any repository, but could be made available legally by the author.
Full text: Unavailable
Published version:
archiving forbidden
Data provided by 