Gene conversion in incontinentia pigmenti: a Chinese case series
Abstract Incontinentia pigmenti (IP) is a rare X-linked dominant condition that leads to variable abnormalities affecting the skin, hair, nails, teeth, eyes, and central nervous system. It is associated with variants in the IKBKG (also known as NEMO) gene, and recent findings have identified gene co...
Salvato in:
| Autori principali: | , , , , , , |
|---|---|
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Springer
2025-06-01
|
| Serie: | Journal of Rare Diseases |
| Soggetti: | |
| Accesso online: | https://doi.org/10.1007/s44162-025-00081-2 |
| Tags: |
Nessun Tag, puoi essere il primo ad aggiungerne!!
|