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A novel loss-of-function mutation in Npr2 clarifies primary role in female reproduction and reveals a potential therapy for acromesomelic dysplasia, Maroteaux type
Geister, K. A., Brinkmeier, M. L., Hsieh, M., Faust, S. M., Karolyi, I. J., Perosky, J. E., Kozloff, K. M., Conti, M., Camper, S. A.Volume:
22
Language:
english
Journal:
Human Molecular Genetics
DOI:
10.1093/hmg/dds432
Date:
January, 2013
File:
PDF, 620 KB
english, 2013