Wikidata

(Q42595317)

English

Genetic analysis in patients with Kallmann syndrome: coexistence of mutations in prokineticin receptor 2 and KAL1.

scientific article published on 21 August 2008

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Statements

title
Genetic analysis in patients with Kallmann syndrome: coexistence of mutations in prokineticin receptor 2 and KAL1. (English)
1 reference
stated in
Europe PubMed Central
PubMed ID
18723471
retrieved
3 November 2017
publication date
21 August 2008
1 reference
stated in
Europe PubMed Central
PubMed ID
18723471
retrieved
3 November 2017

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