Children with ocular motor apraxia type Cogan carry deletions in the gene (NPHP1) for juvenile nephronophthisis (Q28145773)
Jump to navigation
Jump to search
scientific article (publication date: June 2000)
Language | Label | Description | Also known as |
---|---|---|---|
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
June 2000
0 references
136
0 references
6
0 references
828-31
0 references