SUN-074 Loss-Of-Function Mutations in GATA4 in Patients with 46,XY Disorders of Sex Development Without Cardiac Defects

Background: Disorders of sex development (DSD) encompass a wide range of conditions associated with numerous causative genes. In about 50-60% of 46,XY DSD individuals, the underlying molecular cause remains uncertain. GATA4 haploinsufficiency has been described in patients with congenital heart defe...

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Detalles Bibliográficos
Autores principales: Lee, Yena, Oh, Arum, Yoo, Han-Wook, Choi, Jin-Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Pediatric Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7209421/
http://dx.doi.org/10.1210/jendso/bvaa046.714

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7209421/
http://dx.doi.org/10.1210/jendso/bvaa046.714

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