Genetic Analysis in Patients With Kallmann Syndrome: Coexistence of Mutations in Prokineticin Receptor 2 and KAL1

Title
Genetic Analysis in Patients With Kallmann Syndrome: Coexistence of Mutations in Prokineticin Receptor 2 and KAL1
Authors
Keywords
-
Journal
JOURNAL OF ANDROLOGY
Volume 30, Issue 1, Pages 41-45
Publisher
Wiley
Online
2008-12-03
DOI
10.2164/jandrol.108.005314

Ask authors/readers for more resources

Discover Peeref hubs

Discuss science. Find collaborators. Network.

Join a conversation

Find the ideal target journal for your manuscript

Explore over 38,000 international journals covering a vast array of academic fields.

Search