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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Syndrome and CLCN4[original query]
Locus heterogeneity of Dent's disease: OCRL1 and TMEM27 genes in patients with no CLCN5 mutations.
Pediatric nephrology (Berlin, Germany) 2009 Oct 24 (10): 1967-73.
Tosetto Enrica, Addis Maria, Caridi Gianluca, Meloni Cristiana, Emma Francesco, Vergine Gianluca, Stringini Gilda, Papalia Teresa, Barbano Giancarlo, Ghiggeri Gian Marco, Ruggeri Laura, Miglietti Nunzia, D Angelo Angela, Melis Maria Antonietta, Anglani Fran
Novel mutations and phenotypes of epilepsy-associated genes in epileptic encephalopathies.
Genes, brain, and behavior 2018 Jan .
Zhou P, He N, Zhang J-W, Lin Z-J, Wang J, Yan L-M, Meng H, Tang B, Li B-M, Liu X-R, Shi Y-W, Zhai Q-X, Yi Y-H, Liao W
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