(Q44441923)
Statements
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Novel COL4A4 splice defect and in-frame deletion in a large consanguine family as a genetic link between benign familial haematuria and autosomal Alport syndrome (English)
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Novel COL4A4 splice defect and in‐frame deletion in a large consanguine family as a genetic link between benign familial haematuria and autosomal Alport syndrome (English)
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Kai-Olaf Netzer
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Romy Lambrecht
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Stefan Seibold
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Manfred Weber
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1 June 2003
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18
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6
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1122-1127
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Identifiers
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