Exome Sequencing Identifies Truncating Mutations in Human SERPINF1 in Autosomal-Recessive Osteogenesis Imperfecta - Concepedia

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Exome Sequencing Identifies Truncating Mutations in Human SERPINF1 in Autosomal-Recessive Osteogenesis Imperfecta

DOI Full Paper Access

354

Citations

48

References

2011

Year

Jutta Becker, Oliver Semler, Christian Gilissen, Yun Li, Hanno J. Bolz, Cecilia Giunta, Carsten Bergmann, Marianne Rohrbach, Friederike Koerber, Katharina Zimmermann,

The American Journal of Human Genetics

SclerostinDevelopmental BiologyMendelian DisorderGenetic DisorderHuman Serpinf1GeneticsOsteogenesisMolecular GeneticsAutosomal-recessive Osteogenesis ImperfectaDisease Gene IdentificationGenomicsMedicineOsteoporosis

References

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