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Mutations within The Transcription Factor PROP1 in a Cohort of Turkish Patients with Combined Pituit...

Mutations within The Transcription Factor PROP1 in a Cohort of Turkish Patients with Combined Pituit...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_834c2557d203484c97842279ba83d755

Mutations within The Transcription Factor PROP1 in a Cohort of Turkish Patients with Combined Pituitary Hormone Deficiency

About this item

Full title

Mutations within The Transcription Factor PROP1 in a Cohort of Turkish Patients with Combined Pituitary Hormone Deficiency

Publisher

Turkey: Galenos Yayinevi Tic. Ltd

Journal title

Journal of clinical research in pediatric endocrinology, 2020-09, Vol.12 (3), p.261-268

Language

English

Formats

Publication information

Publisher

Turkey: Galenos Yayinevi Tic. Ltd

More information

Scope and Contents

Contents

Mutations of genes encoding transcription factors which play important roles in pituitary morphogenesis, differentiation and maturation lead to combined pituitary hormone deficiency (CPHD).
gene mutations are reported as the most frequent genetic aetiology of CHPD. The aim of this study is to describe phenotype of Turkish CPHD patients and defin...

Alternative Titles

Full title

Mutations within The Transcription Factor PROP1 in a Cohort of Turkish Patients with Combined Pituitary Hormone Deficiency

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_834c2557d203484c97842279ba83d755

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_834c2557d203484c97842279ba83d755

Other Identifiers

ISSN

1308-5727

E-ISSN

1308-5735

DOI

10.4274/jcrpe.galenos.2020.2019.0191

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