A carregar...
CHMP4B, a Novel Gene for Autosomal Dominant Cataracts Linked to Chromosome 20q
Cataracts are a clinically diverse and genetically heterogeneous disorder of the crystalline lens and a leading cause of visual impairment. Here we report linkage of autosomal dominant “progressive childhood posterior subcapsular” cataracts segregating in a white family to short tandem repeat (STR)...
Na minha lista:
| Main Authors: | , , , , , , , |
|---|---|
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The American Society of Human Genetics
2007
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1950844/ https://ncbi.nlm.nih.gov/pubmed/17701905 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|