Supplementary information

From the following article

Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta

Wayne A Cabral, Weizhong Chang, Aileen M Barnes, MaryAnn Weis, Melissa A Scott, Sergey Leikin, Elena Makareeva, Natalia V Kuznetsova, Kenneth N Rosenbaum, Cynthia J Tifft, Dorothy I Bulas, Chahira Kozma, Peter A Smith, David R Eyre & Joan C Marini

Nature Genetics 39, 359 - 365 (2007)

doi:10.1038/ng1968

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Supplementary Fig. 1

LEPRE1 mutations in severe recessive osteogenesis imperfecta.

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Supplementary Fig. 2

Identification of leprecan in the extracellular matrix of murine bone.

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Supplementary Table 1

PCR primers for mutation analysis and transcript structure determination.

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Supplementary Note

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