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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 9, 2024. (Total: 232364Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Sclerosis and PLCE1[original query]
Exclusion of homozygous PLCE1 (NPHS3) mutations in 69 families with idiopathic and hereditary FSGS.
Pediatric nephrology (Berlin, Germany) 2009 Feb 24 (2): 281-5.
Gbadegesin Rasheed, Bartkowiak Bartlomiej, Lavin Peter J, Mukerji Nirvan, Wu Guanghong, Bowling Brandy, Eckel Jason, Damodaran Tirupapuliyur, Winn Michelle
The Frequency of Genetic Mutations in Pediatric Patients Diagnosed with Nephrotic Syndrome: A Single-Center Retrospective Study in Saudi Arabia.
Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia 2022 2 32 (3): 798-805.
Almokali Khamisa, Alyami Ali, Ajeebi Abdulaziz, Almutairi Turki, Aldriwesh Mar
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