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Comment

. 2011 Aug;80(2):136-7.

doi: 10.1111/j.1399-0004.2011.01702.x. Epub 2011 Jun 13.

A step forward on the path towards understanding osteoporosis

E Fisher¹

Affiliations

Affiliation

¹ Centre for Molecular Medicine and Therapeutics, Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, V5Z 4H4 Canada. emilyf@cmmt.ubc.ca

PMID: 21564092
DOI: 10.1111/j.1399-0004.2011.01702.x

Comment

A step forward on the path towards understanding osteoporosis

E Fisher. Clin Genet. 2011 Aug.

. 2011 Aug;80(2):136-7.

doi: 10.1111/j.1399-0004.2011.01702.x. Epub 2011 Jun 13.

Author

E Fisher¹

Affiliation

¹ Centre for Molecular Medicine and Therapeutics, Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, V5Z 4H4 Canada. emilyf@cmmt.ubc.ca

PMID: 21564092
DOI: 10.1111/j.1399-0004.2011.01702.x

No abstract available

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Mutations in NOTCH2 cause Hajdu-Cheney syndrome, a disorder of severe and progressive bone loss.
Simpson MA, Irving MD, Asilmaz E, Gray MJ, Dafou D, Elmslie FV, Mansour S, Holder SE, Brain CE, Burton BK, Kim KH, Pauli RM, Aftimos S, Stewart H, Kim CA, Holder-Espinasse M, Robertson SP, Drake WM, Trembath RC. Simpson MA, et al. Nat Genet. 2011 Mar 6;43(4):303-5. doi: 10.1038/ng.779. Nat Genet. 2011. PMID: 21378985

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