Work

Identification of a novel mutation of the PRKAR1A gene in a patient with Carney complex with significant osteoporosis and recurrent fractures

Year: 2015

Type: article

Study design: Case Report

Source: HORMONES

DOI: 10.14310/horm.2002.1627

Authors: Labrini Papanastasiou, Stelios Fountoulakis, Nikos Voulgaris, Theodora Kounadi, Theodosia Choreftaki, Akrivi Kostopoulou, George Zografos, Charalampos Lyssikatos, Constantine Stratakis, George Piaditis

Institutions: General Hospital of Athens G. Genimatas, National Institutes of Health, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Language: English

Topic: Bone Tumor Diagnosis and Treatments

Subfield: Rheumatology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: bronze

Funders: National Institutes of Health, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: G5010008341, Molecular Genetics Of Adrenocortical Tumors And Related Disorders, Molecular Genetics Of Adrenocortical Tumors And Related Disorders

OpenAlex ID: W2345066212

FWCI: 0.84

Cites: 26

Cited by: 9

Related to: 10