(Q28145773)

English

Children with ocular motor apraxia type Cogan carry deletions in the gene (NPHP1) for juvenile nephronophthisis

scientific article (publication date: June 2000)

Statements

Children with ocular motor apraxia type Cogan carry deletions in the gene (NPHP1) for juvenile nephronophthisis (English)
0 references
R Betz
0 references
C Rensing
0 references
E Otto
0 references
A Mincheva
0 references
D Zehnder
0 references
P Lichter
0 references
F Hildebrandt
0 references
June 2000
0 references
136
0 references
828-31
0 references
6
0 references

Identifiers

0 references
 
edit
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit