A carregar...
Two novel SASH1 mutations in Chinese families with dyschromatosis universalis hereditaria
BACKGROUND: Dyschromatosis universalis hereditaria (DUH) is a rare genodermatosis characterized by hyper‐ and hypo‐pigmented macules on the face, trunk, and extremities. The condition causes severe cosmetic problem which can lead to significant psychological distress to the patients and bear a negat...
Na minha lista:
| Publicado no: | J Clin Lab Anal |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2021
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8183922/ https://ncbi.nlm.nih.gov/pubmed/34028087 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jcla.23803 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|