Osteoporosis in late-diagnosed adult homocystinuric patients
Author:
Affiliation:
1. ; Laboratoire de Biochimie; Hôpital Pellegrin; Bordeaux France
2. ; Service de Pediatrie; Hôpital Pellegrin; Bordeaux France
3. Service de Nutrition et Maladies Métaboliques Hôpital Haut-Lévêque; Pessac France
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1005618927729/fullpdf
Reference4 articles.
1. Evidence for McKusick's hypothesis of deficient collagen cross-linking in patients with homocystinuria;Lubec;Biochim Biophys Acta,1996
2. The natural history of homocystinuria due to cystathionine-β-synthase deficiency;Mudd;Am J Hum Genet,1985
3. Homocystinuria due to cystathionine-β-synthase deficiency in Ireland: 25 years experience of a newborn screened and treated population with reference to clinical outcome and biochemical control;Yap;J Inherit Metab Dis,1998
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