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Homozygous mutation in the prokineticin-receptor2 gene (Val274Asp) presenting as reversible Kallmann syndrome and persistent oligozoospermia: Case Report
Sinisi, A. A., Asci, R., Bellastella, G., Maione, L., Esposito, D., Elefante, A., De Bellis, A., Bellastella, A., Iolascon, A.Volume:
23
Language:
english
Journal:
Human Reproduction
DOI:
10.1093/humrep/den247
Date:
July, 2008
File:
PDF, 172 KB
english, 2008