Literature DB >> 24703149

Re: Identification of HESX1 mutations in Kallmann syndrome.

Craig Niederberger.   

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Year:  2014        PMID： 24703149     DOI： 10.1016/j.juro.2014.01.067

Source DB:  PubMed          Journal:  J Urol        ISSN： 0022-5347            Impact factor:   7.450


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  1 in total

1.  Study on KAL1 Gene Mutations in Idiopathic Hypogonadotropic Hypogonadism Patients with X-Linked Recessive Inheritance.

Authors:  Atefeh Ahmadzadeh; Elahe Ghods; Majid Mojarrad; Robab Aboutorabi; Mojgan Afkhamizadeh; Shokoofeh Bonakdaran; Zohreh Mosavi; Seyed Morteza Taghavi; Mohammad Hassanzadeh Nazarabadi
Journal:  Int J Mol Cell Med       Date:  2015
  1 in total

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