Two novel fibrillin-2 mutations in congenital contractural arachnodactyly
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference28 articles.
1. A single mutation that results in an Asp to His substitution and partial exon skipping in a family with congenital contractural arachnodactyly
2. Congenital Contractural Arachnodactyly
3. Congenital Contractural Arachnodactyly
4. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction
5. Mutations in the human gene for fibrillin-1 (FBN1) in the Marfan syndrome and related disorders
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