(Q24669843)

English

Homozygous nonsense mutation in the FOXE3 gene as a cause of congenital primary aphakia in humans

scientific article

Statements

Homozygous nonsense mutation in the FOXE3 gene as a cause of congenital primary aphakia in humans (English)
0 references
0 references
0 references
Florence Niel
0 references
Marie-Paule Algros
0 references
Claire Schwartz
0 references
Bernard Delbosc
0 references
Marc Delpech
0 references
Bernadette Kantelip
0 references
August 2006
0 references
79
0 references
2
0 references
358-64
0 references

Identifiers

 
edit
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit