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Renal Phenotype Variations among Families with Autosomal Alport Syndrome: Potential Role of Modifier Genes.

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Bibliographic Details
Title:	Renal Phenotype Variations among Families with Autosomal Alport Syndrome: Potential Role of Modifier Genes.
Authors:	Ibrahim A; Nephrology Division, Internal Medicine Department, University of Utah Health, Salt Lake City, Utah., Lin E; Internal Medicine Department, University of Utah Health, Salt Lake City, Utah., Hinckley M; Nephrology Division, Internal Medicine Department, University of Utah Health, Salt Lake City, Utah., Khalighi M; Dermatology Department, University of Utah Health, Salt Lake City, Utah., Altawallbeh Z; Nephrology Division, Internal Medicine Department, University of Utah Health, Salt Lake City, Utah., Al-Rabadi D; Faculty of Medicine, Jordan University of Science and Technology, Irbid, Jordan., Al-Hassanat Z; Faculty of Medicine, Jordan University of Science and Technology, Irbid, Jordan., Pezzolesi MG; Nephrology Division, Internal Medicine Department, University of Utah Health, Salt Lake City, Utah., Gregory MC; Nephrology Division, Internal Medicine Department, University of Utah Health, Salt Lake City, Utah., Al-Rabadi L; Nephrology Division, Internal Medicine Department, University of Utah Health, Salt Lake City, Utah.
Source:	Kidney360 [Kidney360] 2025 May 01; Vol. 6 (5), pp. 824-834. Date of Electronic Publication: 2025 Feb 14.
Publication Type:	Journal Article
Journal Info:	Publisher: Wolters Kluwer Health, Inc. on behalf of the American Society of Nephrology Country of Publication: United States NLM ID: 101766381 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2641-7650 (Electronic) Linking ISSN: 26417650 NLM ISO Abbreviation: Kidney360 Subsets: MEDLINE; In Process
Database:	MEDLINE Ultimate

Description
ISSN:	2641-7650
DOI:	10.34067/KID.0000000722