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A deletion mutation in TMEM38B associated with autosomal recessive osteogenesis imperfecta

Michael Volodarsky1, Barak Markus, Idan Cohen

  • 1The Morris Kahn Laboratory of Human Genetics at the National Institute for Biotechnology in the Negev (NIBN) and Faculty of Health Sciences, Ben Gurion University, Beer-Sheva, Israel.

Human Mutation
|January 15, 2013
PubMed

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