A recurrent mutation in type II collagen gene causes Legg-Calvé-Perthes disease in a Japanese family-Reference-Cited by-同舟云学术

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A recurrent mutation in type II collagen gene causes Legg-Calvé-Perthes disease in a Japanese family

Published:2007-03-30 Issue:5 Volume:121 Page:625-629
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Miyamoto Yoshinari,Matsuda Tatsuo,Kitoh Hiroshi,Haga Nobuhiko,Ohashi Hirofumi,Nishimura Gen,Ikegawa Shiro

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-007-0354-y.pdf

Reference21 articles.

1. Caffey J (1968) The early roentgenographic changes in essential coxa plana: their significance in pathogenesis. Am J Roentgenol Radium Ther Nucl Med 103:620–634

2. Catterall A (1971) The natural history of Perthes’ disease. J Bone Joint Surg Br 53:37–53

3. Chen WM, Liu YF, Lin MW, Chen IC, Lin PY, Lin GL, Jou YS, Lin YT, Fann CS, Wu JY, Hsiao KJ, Tsai SF (2004) Autosomal dominant avascular necrosis of femoral head in two Taiwanese pedigrees and linkage to chromosome 12q13. Am J Hum Genet 75:310–317

4. Dilley A, Hooper WC, Austin H, Jamil M, Miller C, Stokes M, Evatt B, Eldridge J (2003) The beta fibrinogen gene G-455-A polymorphism is a risk factor for Legg-Perthes disease. J Thromb Haemost 1:2317–2321

5. Glueck CJ, Crawford A, Roy D, Freiberg R, Glueck H, Stroop D (1996) Association of antithrombotic factor deficiencies and hypofibrinolysis with Legg-Perthes disease. J Bone Joint Surg Am 78:3–13

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