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Phenotypic heterogeneity associated with the splicing mutation in congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
J Clin Endocrinol Metab. 1996 Nov;81(11):4081-8. doi: 10.1210/jcem.81.11.8923864.
J Clin Endocrinol Metab. 1996.
PMID: 8923864
Human type II arginase: sequence analysis and tissue-specific expression.
Morris SM Jr, Bhamidipati D, Kepka-Lenhart D.
Morris SM Jr, et al.
Gene. 1997 Jul 9;193(2):157-61. doi: 10.1016/s0378-1119(97)00099-1.
Gene. 1997.
PMID: 9256072
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