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Alport Syndrome Genetics:     more detail

Molecular Pathology and Genetics of Alport Syndrome (Contributions to Nephrology) The Molecular Genetics of X-Linked Alport Syndrome (Acta Biomedica Lovaniensia) by Caiying Guo, 1995-11 Familial nephritis: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Maria, PhD Basile, 2005 Hereditary nephropathy with hearing loss: "Alport's syndrome" (Acta paediatrica Scandinavica : Supplement) by Ulla Marianne Iversen, 1974

lists with details

1. Alport Syndrome Foundation - Hope | Action | Support
   The genetics of Alport Syndrome, an inherited kidney disease. Symptoms include blood in urine, hearing loss and anterior lenticonus.  
   http://www.alportsyndrome.org/alport-sub/alport_syndrome_genetics.html
   
   Extractions: ADAS Mode of Inheritance Prenatal testing is available for XLAS and ARAS and may be available for ADAS by laboratories offering custom prenatal testing. See Diagnostic Labs for more information on testing. The 501(c)(3) non-profit Alport Syndrome Foundation is dedicated to educating and supporting patients and families with this genetic kidney disease.

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