Clinical Exome Sequencing Reveals MKRN3 Pathogenic Variants in Familial and Nonfamilial Idiopathic Central Precocious Puberty

Publisher： Karger

E-ISSN： 1663-2826|87|2|88-94

ISSN： 1663-2818

Source： Hormone Research in Paediatrics, Vol.87, Iss.2, 2016-12, pp. : 88-94

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

MKRN3 Mutations in Familial Central Precocious Puberty

By  

Hormone Research in Paediatrics, Vol. 82, Iss. 2, 2014-07 ,pp. : 122-126

Karger

Access to resources Recommend Favorite

Two Frameshift Mutations in MKRN3 in Turkish Patients with Familial Central Precocious Puberty

By  

Hormone Research in Paediatrics, Vol. 87, Iss. 6, 2016-11 ,pp. : 405-411

Karger

Access to resources Recommend Favorite

High Frequency of MKRN3 Mutations in Male Central Precocious Puberty Previously Classified as Idiopathic

By  

Neuroendocrinology, Vol. 105, Iss. 1, 2016-05 ,pp. : 17-25

Karger

Access to resources Recommend Favorite

Time Course of Central Precocious Puberty Development Caused by an MKRN3 Gene Mutation: A Prismatic Case

By  

Hormone Research in Paediatrics, Vol. 86, Iss. 2, 2016-07 ,pp. : 126-130

Karger

Access to resources Recommend Favorite

Absence of GPR54 and TACR3 Mutations in Sporadic Cases of Idiopathic Central Precocious Puberty

By  

Hormone Research in Paediatrics, Vol. 81, Iss. 3, 2014-01 ,pp. : 177-181

Karger

Access to resources Recommend Favorite