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Human Molecular Genetics, Vol. 6, Iss. 5, 1997-01 ,pp. : 805-811

Oxford University Press

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Germinal and somatic mutations in the PKD2 gene of renal cysts in autosomal dominant polycystic kidney disease

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Characterisation of Renal Chloride Channel, CLCN5 , Mutations in Hypercalciuric Nephrolithiasis (Kidney Stones) Disorders

By Lloyd Sarah E.  

Human Molecular Genetics, Vol. 6, Iss. 8, 1997-01 ,pp. : 1233-1239

Oxford University Press

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Mutations in the RP1 gene causing autosomal dominant retinitis pigmentosa

By Bowne Sara J.   Daiger Stephen P.   Hims Matthew M.  

Human Molecular Genetics, Vol. 8, Iss. 11, 1999-10 ,pp. : 2121-2128

Oxford University Press

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The rs3737964 single‐nucleotide polymorphism of the chloride channel‐6 gene as a risk factor for coronary heart disease

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Molecular Genetics & Genomic Medicine, Vol. 3, Iss. 6, 2015-11 ,pp. : 537-542

John Wiley & Sons Inc

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