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The Journal of Clinical Endocrinology and Metabolism|January 13, 2004
A novel nonsense mutation of the mineralocorticoid receptor gene in a Swedish family with pseudohypoaldosteronism type I (PHA1)A-M Nyström, M-L Bondeson, N Skanke, et al.
Developmental Medicine and Child Neurology|January 1, 1995
Neurological dysfunction above cele level in children with spina bifida cystica: a prospective study to three yearsM Dahl, G Ahlsten, H Carlson, et al.
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