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Fox–Fordyce disease in monozygotic female twins

✍ Scribed by Marcelo Massaki Guiotoku; Paula Tardim Lopes; Mariângela Esther Alencar Marques; Silvio Alencar Marques; Hélio Amante Miot

Book ID: 116586528
Publisher: Elsevier Science
Year: 2011
Tongue: English
Weight: 344 KB
Volume: 65
Category: Article
ISSN: 1097-6787
DOI: 10.1016/j.jaad.2009.11.591

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## Abstract Wilson's disease (WD) is an autosomal recessive disorder characterized by the functional disruption of the copper‐transporting protein adenosine triphosphatase 7B (ATP‐ase 7B). The disease is caused by mutations in __ATP7B__ gene. It seems that the type of mutation in __ATP7B__ only to