Deficiency in GALT causes classical galactosaemia Type 1 in autosomal dominant form, which resulted POI as the most common long-term complication [58]. Although, the possible effects of single heterozygous variants is still a question of debate as several examples exist in the literature that ...
Long-term outcome of idiopathic steroid-resistant nephrotic syndrome: a multicenter study. Pediatr Nephrol. 2009;24:1525–32. Article Google Scholar Ding WY, Koziell A, McCarthy HJ, Bierzynska A, Bhagavatula MK, Dudley JA, Inward CD, Coward RJ, Tizard J, Reid C, Antignac C, Boyer O...