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  See also:


http://www.orpha.net/data/patho/GB/uk-CNF.pdf
» Congenital Nephrotic Syndrome, Finnish Type - Orphanet description of the disease by Professor Patrick Niaudet. [PDF]

http://hmg.oxfordjournals.org/cgi/reprint/13/21/2625.pdf
» Human Laminin β2 Deficiency Causes Congenital Nephrosis with Mesangial Sclerosis and Distinct Eye Abnormalities - Full text of paper by Zenker et al. [PDF]

http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=256300
» Online Mendelian Inheritance in Man - Detailed references and diagnostic information.


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