Log in to save to my catalogue

CCDC141 Mutations in Idiopathic Hypogonadotropic Hypogonadism

CCDC141 Mutations in Idiopathic Hypogonadotropic Hypogonadism

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5470764

CCDC141 Mutations in Idiopathic Hypogonadotropic Hypogonadism

About this item

Full title

CCDC141 Mutations in Idiopathic Hypogonadotropic Hypogonadism

Publisher

Washington, DC: Endocrine Society

Journal title

The journal of clinical endocrinology and metabolism, 2017-06, Vol.102 (6), p.1816-1825

Language

English

Formats

Publication information

Publisher

Washington, DC: Endocrine Society

More information

Scope and Contents

Contents

Context:Gonadotropin-releasing hormone neurons originate outside the central nervous system in the olfactory placode and migrate into the central nervous system, becoming integral components of the hypothalamic-pituitary-gonadal axis. Failure of this migration can lead to idiopathic hypogonadotropic hypogonadism (IHH)/Kallmann syndrome (KS). We hav...

Alternative Titles

Full title

CCDC141 Mutations in Idiopathic Hypogonadotropic Hypogonadism

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5470764

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5470764

Other Identifiers

ISSN

0021-972X

E-ISSN

1945-7197

DOI

10.1210/jc.2016-3391

How to access this item