1. Academic Validation
  2. TGFB1 mutations in four new families with Camurati-Engelmann disease: confirmation of independently arising LAP-domain-specific mutations

TGFB1 mutations in four new families with Camurati-Engelmann disease: confirmation of independently arising LAP-domain-specific mutations

  • Am J Med Genet A. 2004 May 15;127A(1):104-107. doi: 10.1002/ajmg.a.20671.
Akira Kinoshita 1 2 3 Yasuyuki Fukumaki 1 Shuya Shirahama 4 Akira Miyahara 4 Gen Nishimura 5 Nobuhiko Haga 6 Atsushi Namba 7 Hitoshi Ueda 8 Hiromi Hayashi 9 Shiro Ikegawa 10 Joerg Seidel 11 Norio Niikawa 2 3 Koh-Ichiro Yoshiura 2 3
Affiliations

Affiliations

  • 1 Division of Disease Genes, Research Center for Genetic Information, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
  • 2 Department of Human Genetics, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan.
  • 3 CREST, Japan Science and Technology Corporation, Kawaguchi, Japan.
  • 4 Center for Molecular Biology and Cytogenetics, SRL, Inc., Tokyo, Japan.
  • 5 Department of Radiology, Tokyo Metropolitan Kiyose Children's Hospital, Tokyo, Japan.
  • 6 Department of Pediatric Orthopedics, Shizuoka Children's Hospital, Shizuoka, Japan.
  • 7 Department of Otorhinolaryngology, Hirosaki University School of Medicine, Hirosaki, Japan.
  • 8 Division of Pediatric Neurology, Osaka Medical Center and Research for Maternal and Child Health, Osaka, Japan.
  • 9 Department of Community and General Medicine, Sapporo Medical University, Sapporo, Japan.
  • 10 Laboratory for Bone and Joint Diseases, SNP Research Center, RIKEN, Tokyo, Japan.
  • 11 Department of Pediatrics and Clinical Genetics, Friedrich-Schiller University of Jena, Jena, Germany.
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