Carrier assessment in families with lowe oculocerebrorenal syndrome: novel mutations in the OCRL1 gene and correlation of direct DNA diagnosis with ocular examination. (Q54055330)
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scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Carrier assessment in families with lowe oculocerebrorenal syndrome: novel mutations in the OCRL1 gene and correlation of direct DNA diagnosis with ocular examination. |
scientific article |
Statements
Carrier assessment in families with lowe oculocerebrorenal syndrome: novel mutations in the OCRL1 gene and correlation of direct DNA diagnosis with ocular examination. (English)
W Röschinger
A C Muntau
G Rudolph
A A Roscher
S Kammerer
1 March 2000
69
3
213-222