Highly variable clinical phenotype of carbamylphosphate synthetase 1 deficiency in one family: an effect of allelic variation in gene expression?
Klaus, V, Vermeulen, T, Minassian, B, Israelian, N, Engel, K, Lund, AM, Roebrock, K, Christensen, E, Häberle, J
Published in Clinical genetics (01.09.2009)
Published in Clinical genetics (01.09.2009)
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