X-linked Alport syndrome with "empty capsule sign"
Kidney Int
.
2020 Feb;97(2):426.
doi: 10.1016/j.kint.2019.08.025.
Authors
Satoru Kudose
1
,
Ibrahim Batal
1
,
Cynthia D'Alessandri-Silva
2
,
Fangming Lin
3
,
Vivette D D'Agati
1
,
Glen S Markowitz
4
Affiliations
1
Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, New York, USA.
2
Department of Nephrology, Connecticut Children's Medical Center, Hartford, Connecticut, USA.
3
Department of Pediatrics, Columbia University Irving Medical Center, New York, New York, USA.
4
Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, New York, USA. Electronic address:
[email protected]
.
PMID:
31980082
DOI:
10.1016/j.kint.2019.08.025
No abstract available
MeSH terms
Collagen Type IV / genetics
Humans
Kidney
Nephritis, Hereditary* / diagnosis
Nephritis, Hereditary* / genetics
Substances
Collagen Type IV