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Publication | Open Access

Time Course of Central Precocious Puberty Development Caused by an <b><i>MKRN3</i></b> Gene Mutation: A Prismatic Case

DOIFull Paper Access

21

Citations

15

References

2016

Year

Mônica Freire Stecchini, Delanie B. Macedo, Ana Claudia S. Reis, Ana Paula Abreu, Ayrton Custódio Moreira, Margaret de Castro, Ursula B. Kaiser, Ana Cláudia Latronico, Sonir Roberto Rauber Antonini
Hormone Research in Paediatrics

Abstract

The identification of carriers of MKRN3 mutations may contribute to early diagnosis of CPP, facilitating treatment decisions and guiding genetic counseling and prompt intervention in familial cases.

References

YearCitations

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