PROKR2 and PROK2 mutations cause isolated congenital anosmia without gonadotropic deficiency
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Title
PROKR2 and PROK2 mutations cause isolated congenital anosmia without gonadotropic deficiency
Authors
Keywords
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Journal
EUROPEAN JOURNAL OF ENDOCRINOLOGY
Volume 168, Issue 1, Pages 31-37
Publisher
Bioscientifica
Online
2012-10-19
DOI
10.1530/eje-12-0578
References
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- The Role of the Prokineticin 2 Pathway in Human Reproduction: Evidence from the Study of Human and Murine Gene Mutations
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- Heparan sulfate 6-O-sulfotransferase 1, a gene involved in extracellular sugar modifications, is mutated in patients with idiopathic hypogonadotrophic hypogonadism
- (2011) J. Tornberg et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
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- (2010) Luis Teixeira et al. JOURNAL OF CLINICAL INVESTIGATION
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- (2010) G. P. Sykiotis et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- A Comparative Phenotypic Study of Kallmann Syndrome Patients Carrying Monoallelic and Biallelic Mutations in the Prokineticin 2 or Prokineticin Receptor 2 Genes
- (2009) Julie Sarfati et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
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- (2008) Carine Monnier et al. HUMAN MOLECULAR GENETICS
- Loss-of-Function Mutations in the Genes Encoding Prokineticin-2 or Prokineticin Receptor-2 Cause Autosomal Recessive Kallmann Syndrome
- (2008) Ana Paula Abreu et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Mutations inProkineticin 2andProkineticin receptor 2genes in Human Gonadotrophin-Releasing Hormone Deficiency: Molecular Genetics and Clinical Spectrum
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- (2007) Allan E. Herbison et al. ENDOCRINOLOGY
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