Progress and Current Status in Hajdu-Cheney Syndrome with Focus on Novel Genetic Research

Hajdu-Cheney syndrome (HCS) is a rare autosomal dominant manifestation of a congenital genetic disorder caused by a mutation in the NOTCH2 gene. NOTCH signaling has variations from NOTCH 1 to 4 and maintains homeostasis by determining and regulating the proliferation and differentiation of various c...

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Detalles Bibliográficos
Autores principales: Aida, Natsuko, Ohno, Tatsukuni, Azuma, Toshifumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9570194/
https://www.ncbi.nlm.nih.gov/pubmed/36232677
http://dx.doi.org/10.3390/ijms231911374

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9570194/
https://www.ncbi.nlm.nih.gov/pubmed/36232677
http://dx.doi.org/10.3390/ijms231911374

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