Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism?

Imprinting disorders are congenital diseases caused by dysregulation of genomic imprinting, affecting growth, neurocognitive development, metabolism and cancer predisposition. Overlapping clinical features are often observed among this group of diseases. In rare cases, two fully expressed imprinting...

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Detalles Bibliográficos
Autores principales: Pignata, Laura, Cecere, Francesco, Acquaviva, Fabio, D’Angelo, Emilia, Cioffi, Daniela, Pellino, Valeria, Palumbo, Orazio, Palumbo, Pietro, Carella, Massimo, Sparago, Angela, De Brasi, Daniele, Cerrato, Flavia, Riccio, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Cell and Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10448386/
https://www.ncbi.nlm.nih.gov/pubmed/37635873
http://dx.doi.org/10.3389/fcell.2023.1237629

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10448386/
https://www.ncbi.nlm.nih.gov/pubmed/37635873
http://dx.doi.org/10.3389/fcell.2023.1237629

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