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Renal-retinal syndromes: Association of retinal anomalies and recessive nephronophthisis in patients with homozygous deletion of the NPH1 locus

✍ Scribed by G Caridi; L Murer; R Bellantuono; P Sorino; DA Caringella; R Gusmano; GM Ghiggeri


Book ID
117444200
Publisher
Elsevier Science
Year
1998
Tongue
English
Weight
49 KB
Volume
32
Category
Article
ISSN
0272-6386

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