COL4A6 is dispensable for autosomal recessive Alport syndrome

COL4A6 is dispensable for autosomal recessive Alport syndrome

10.1038/srep29450

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Bibliographic Details
Main Authors:	Murata, T, Katayama, K, Oohashi, T, Jahnukainen, T, Yonezawa, T, Sado, Y, Ishikawa, E, Nomura, S, Tryggvason, K, Ito, M
Other Authors:	DUKE-NUS MEDICAL SCHOOL
Format:	Article
Published:	Nature Publishing Group 2020
Subjects:	COL4A1 protein, human Col4a1 protein, mouse COL4A2 protein, human Col4a2 protein, mouse COL4A6 protein, human collagen type 4 peptide fragment adolescent animal C57BL mouse cross breeding female genetics glomerulus basement membrane homozygote human intron kidney knockout mouse male metabolism mouse mutation nephritis recessive gene Adolescent Animals Collagen Type IV Crosses, Genetic Female Genes, Recessive Glomerular Basement Membrane Homozygote Humans Introns Kidney Male Mice Mice, Inbred C57BL Mice, Knockout Mutation Nephritis, Hereditary Peptide Fragments
Online Access:	https://scholarbank.nus.edu.sg/handle/10635/182453
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Institution:	National University of Singapore

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