Mutational analysis of patients with the diagnosis of choroideremia
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference24 articles.
1. Recommendations for a nomenclature system for human gene mutations
2. The Protein Truncation Test (PTT) as a Method of Detection for Choroideremia Mutations
3. The CpG dinucleotide and human genetic disease
4. Molecular basis of base substitution hotspots in Escherichia coli
5. Mutation nomenclature extensions and suggestions to describe complex mutations: A discussion
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