Lanean...
A novel large deletion mutation of FERMT1 gene in a Chinese patient with Kindler syndrome
Kindler syndrome (KS; OMIM 173650) is a rare autosomal recessive skin disorder, which results in symptoms including blistering, epidermal atrophy, increased risk of cancer, and poor wound healing. The majority of mutations of the disease-determining gene (FERMT1 gene) are single nucleotide substitut...
Gorde:
| Argitaratua izan da: | J Zhejiang Univ Sci B |
|---|---|
| Egile Nagusiak: | , , , , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Zhejiang University Press
2015
|
| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4642877/ https://ncbi.nlm.nih.gov/pubmed/26537214 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1631/jzus.B1500080 |
| Etiketak: |
Etiketa erantsi
Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!
|