(Q51990765)
Statements
[Clinical findings in a patient with Lowe syndrome and a splice site mutation in the OCRL1 gene]. (English)
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C N Keilhauer
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A Gal
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J E Sold
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J Zimmermann
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K-O Netzer
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L Schramm
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1 March 2007
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224
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3
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207-209
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