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Novel Genetic and Biochemical Findings of DLK1 in Children with Central Precocious Puberty: A Brazilian–Spanish Study

DOIFull Paper Access

48

Citations

23

References

2020

Year

Luciana Ribeiro Montenegro, José Ignacio Labarta, Ana Pinheiro Machado Canton, Raquel Corripio, Leandro Soriano‐Guillén, Lourdes Travieso‐Suárez, Álvaro Martín‐Rivada, Vicente Barrios, Carlos Eduardo Seraphim, Vinícius Nahime Brito,
The Journal of Clinical Endocrinology & Metabolism

Abstract

Loss-of-function mutations of DLK1 represent a rare cause of CPP, reinforcing a significant role of this factor in human pubertal timing.

References

YearCitations

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