A progressive cone-rod dystrophy and amelogenesis imperfecta: a new syndrome.
AUTOR(ES)
Jalili, I K
RESUMO
Twenty-nine members of an extended Arab family from the Gaza Strip were found to be affected with cone-rod dystrophy and amelogenesis imperfecta, inherited in an autosomal recessive manner.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1051576Documentos Relacionados
- Cone and cone-rod dystrophies.
- Vitreous fluorophotometry in patients with cone-rod dystrophy.
- Autosomal dominant cone-rod dystrophy with negative electroretinogram.
- Genetic enhancement of cognition in a kindred with cone–rod dystrophy due to RIMS1 mutation
- Microsatellite markers for the cone-rod retinal dystrophy gene, CRX, on 19q13.3.
