A novel GNRHR gene mutation causing congenital hypogonadotrophic hypogonadism in a Brazilian kindred-Reference-Cited by-同舟云学术

A novel GNRHR gene mutation causing congenital hypogonadotrophic hypogonadism in a Brazilian kindred

Published:2018-12 Issue:12 Volume:30 Page:e12658
ISSN:0953-8194
Container-title:Journal of Neuroendocrinology
language:en
Short-container-title:J Neuroendocrinol

Author:

Correa-Silva Silvia Regina¹^ORCID,Fausto Jessica da Silva¹,Kizys Marina Malta Letro¹,Filipelli Rafael²,Marco Antonio David Santos³,Oku Andre Yuji³,Furuzawa Gilberto Koiti¹,Orchard Eugenia Verônica Hernandez⁴,Costa-Barbosa Flavia Amanda¹³^ORCID,Mitne-Neto Miguel³⁵,Dias-da-Silva Magnus R.¹^ORCID

Affiliation:

1. Laboratory of Molecular and Translational Endocrinology; Department of Medicine; Escola Paulista de Medicina; Universidade Federal de São Paulo; São Paulo Brazil

2. Molecular Biology and Lysosomal Disease Diagnosis Laboratory; Department of Biophysics; Escola Paulista de Medicina; Universidade Federal de São Paulo; São Paulo Brazil

3. Research and Development; Fleury Group; São Paulo Brazil

4. Unimed Belo Horizonte; Belo Horizonte Brazil

5. Human Genome and Stem Cell Research Center (HUG-CELL); Biosciences Institute; University of São Paulo (USP); São Paulo Brazil

Funder

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Fundação de Amparo à Pesquisa do Estado de São Paulo

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Endocrine and Autonomic Systems,Endocrinology,Endocrinology, Diabetes and Metabolism

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/jne.12658/fullpdf

Reference36 articles.

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5. Lack of decussation of pyramids in Kallmann syndrome presenting with mirror movements;Vale;J Neurol Sci,2017

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