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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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
Format: Artigo
Sprog:Inglês
Udgivet: American Society for Investigative Pathology 2007
Fag:
Regular Articles
Online adgang: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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