A carregar...
Oculodentodigital dysplasia
Oculodentodigital dysplasia is a rare, autosomal dominant disorder with high penetrance and variable expressivity, caused by mutations in the connexin 43 or gap junction protein alpha-1 gene. It has been diagnosed in fewer than 300 people worldwide with an incidence of around 1 in 10 million. It aff...
Na minha lista:
| Main Authors: | , , , |
|---|---|
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wolters Kluwer Medknow Publications
2016-01-01
|
| Colecção: | Indian Journal of Ophthalmology |
| Assuntos: | |
| Acesso em linha: | http://www.ijo.in/article.asp?issn=0301-4738;year=2016;volume=64;issue=3;spage=227;epage=230;aulast=Doshi |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|