GATA4 mutations are uncommon in patients with 46,XY disorders of sex development without heart anomaly

Asian J Androl. 2018 Nov-Dec;20(6):629-631. doi: 10.4103/aja.aja_20_18.

Authors

Maki Igarashi¹, Kentaro Mizuno², Masafumi Kon¹, Satoshi Narumi¹, Yoshiyuki Kojima³, Yutaro Hayashi², Tsutomu Ogata⁴, Maki Fukami¹

Affiliations

¹ Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo 157-8535, Japan.
² Department of Nephro-Urology, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.
³ Department of Urology, Fukushima Medical University, Fukushima 960-1295, Japan.
⁴ Department of Pediatrics, Hamamatsu University School of Medicine, Hamamatsu 431-3192, Japan.

No abstract available

Publication types

Letter

MeSH terms

Disorder of Sex Development, 46,XY / genetics*
GATA4 Transcription Factor / genetics*
Genetic Testing
Heart Defects, Congenital
Humans
Male
Molecular Structure
Mutation / genetics

Substances

GATA4 Transcription Factor
GATA4 protein, human