Severe Glomerular Endothelial Injury Associated with a Short D4Z4 Repeat on Chromosome 4q35-Reference-Cited by-同舟云学术

Severe Glomerular Endothelial Injury Associated with a Short D4Z4 Repeat on Chromosome 4q35

Published:2017 Issue:14 Volume:56 Page:1849-1853
ISSN:0918-2918
Container-title:Internal Medicine
language:en
Short-container-title:Intern. Med.

Author:

Hibino Satoshi¹,Takeda Asami²,Nishino Ichizo³,Iwata Naoyuki¹,Nakano Masaru¹,Tanaka Kazuki¹,Yamakawa Satoshi¹,Nagai Takuhito¹,Uemura Osamu¹

Affiliation:

1. Pediatric Nephrology, Aichi Children's Health and Medical Center, Japan

2. Department of Nephrology, Nagoya Second Red Cross Hospital, Japan

3. Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Japan

Publisher

Japanese Society of Internal Medicine

Subject

General Medicine,Internal Medicine

Link

https://www.jstage.jst.go.jp/article/internalmedicine/56/14/56_56.7441/_pdf

Reference20 articles.

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2. 2. Reynolds BC, Lemmers RJ, Tolmie J, Howatson AG, Hughes DA. Focal segmental glomerulosclerosis, Coats'-like retinopathy, sensorineural deafness and chromosome 4 duplication: a new association. Pediatr Nephrol 25: 1551-1554, 2010.

3. 3. Brouwer OF, George W, Padberg GW, Wijmenga C, Frants RR. Facioscapulohumeral muscular dystrophy in early childhood. Arch Neurol 51: 387-394, 1994.

4. 4. Funakoshi M, Goto K, Arahata K. Epilepsy and mental retardation in a subset of early onset 4q35 facioscapulohumeral muscular dystrophy. Neurology 50: 1791-1794, 1998.

5. 5. Deidda G, Cacurri S, Grisanti P, Viqneti E, Piazzo N, Felicetti L. Physical mapping evidence for a duplicated region on chromosome 10qter showing high homology with the facioscapulohumeral muscular dystrophy locus on chromosome 4qter. Eur J Hum Genet 3: 155-167, 1995.

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