(Q54055330)
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)
1 reference
W Röschinger
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A C Muntau
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G Rudolph
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A A Roscher
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S Kammerer
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1 March 2000
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69
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3
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213-222
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Identifiers
1 reference