Central precocious puberty in a boy with X-linked adrenoleukodystrophy caused by a novel ABCD1 mutation
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Elsevier BV
Reference22 articles.
1. X-linked adrenoleukodystrophy;Moser;Nat. Clin. Pract. Neurol.,2007
2. Newborn screening for X-linked adrenoleukodystrophy: review of data and outcomes in Pennsylvania;Priestley;Int. J. Neonatal. Screen.,2022
3. Eight novel mutations in the ABCD1 gene and clinical characteristics of 25 Chinese patients with X-linked adrenoleukodystrophy;Chu;World. J. Pediatr.,2015
4. Adrenoleukodystrophy - neuroendocrine pathogenesis and redefinition of natural history;Kemp;Nat. Rev. Endocrinol.,2016
5. The natural history of adrenal insufficiency in X-linked adrenoleukodystrophy: an international collaboration;Huffnagel;J. Clin. Endocrinol. Metab.,2019
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