CYP1B1 Mutation Profile of Iranian Primary Congenital Glaucoma Patients and Associated Haplotypes

The mutation spectrum of CYP1B1 among 104 primary congenital glaucoma patients of the genetically heterogeneous Iranian population was investigated by sequencing. We also determined intragenic single nucleotide polymorphism (SNP) haplotypes associated with the mutations and compared these with haplo...

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Detalhes bibliográficos
Main Authors: Chitsazian, Fereshteh, Tusi, Betsabeh Khoramian, Elahi, Elahe, Saroei, Heidar Amini, Sanati, Mohammad H., Yazdani, Shahin, Pakravan, Mohammad, Nilforooshan, Navid, Eslami, Yadollah, Mehrjerdi, Mohammad Ali Zare, Zareei, Reza, Jabbarvand, Mahmood, Abdolahi, Ali, Lasheyee, Ali R., Etemadi, Arash, Bayat, Behnaz, Sadeghi, Mehdi, Banoei, Mohammad M., Ghafarzadeh, Behnam, Rohani, Mohammad R., Rismanchian, Akram, Thorstenson, Yvonne, Sarfarazi, Mansoor
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Investigative Pathology 2007
Assuntos:
Regular Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1899412/
https://ncbi.nlm.nih.gov/pubmed/17591938
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2353/jmoldx.2007.060157
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