Loss-Of-Function Mutation in the Prokineticin 2 Gene Causes Kallmann Syndrome and Normosmic Idiopathic Hypogonadotropic Hypogonadism

AuthID
 P-004-6QJ
11
Author(s)
Zhang, C
·
Li, JD
·
Cole, LW
·
Plummer, L
·
Jacobson Dickman, EE
·
Mellon, PL
·
Zhou, QY
·
Crowley, WF
Document Type
Article
Year published
2007
Published
in PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, ISSN: 0027-8424
Volume: 104, Issue: 44, Pages: 17447-17452 (6)
Indexing
Wos®
Scopus®
Crossref®190
Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 17959774
SCOPUS: 2-s2.0-36849044530
Wos: WOS:000250638400040
Source Identifiers
ISSN: 0027-8424
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