Rare Variants in the MECP2 Gene in Girls with Central Precocious Puberty

BACKGROUND: Identification of genetic causes of central precocious puberty (CPP) has revealed epigenetic mechanisms as regulators of human pubertal timing. Methyl-CpG-binding protein 2 (MECP2), an X-linked gene, encodes a chromatin-associated protein with a role in gene transcription. MECP2 loss-of-...

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Bibliografske podrobnosti
izdano v:Lancet Diabetes Endocrinol
Main Authors: Canton, Ana P. M., Tinano, Flávia R., Guasti, Leonardo, Montenegro, Luciana R., Ryan, Fiona, Shears, Deborah, de Melo, Maria Edna, Gomes, Larissa G., Piana, Mariana P., Brauner, Raja, Aguilar, Rafael E., Escribano-Munôz, Arancha, Paganoni, Alyssa, Read, Jordan, Korbonits, Márta, Seraphim, Carlos E., Costa, Silvia S., Krepischi, Ana Cristina, Jorge, Alexander A. L., David, Alessia, Kaisinger, Lena R., Ong, Ken K., Perry, John R. B., Abreu, Ana Paula, Kaiser, Ursula B., Argente, Jesús, Mendonca, Berenice B., Brito, Vinicius N., Howard, Sasha R., Latronico, Ana Claudia
Format: Artigo
Jezik:Inglês
Izdano: 2023
Teme:
Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC7615084/
https://ncbi.nlm.nih.gov/pubmed/37385287
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/S2213-8587(23)00131-6
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