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pubmed-article:10369742pubmed:abstractTextThe authors present two new missense mutations in exon 1 of the adrenoleukodystrophy (ALD) gene. The first, a C813T transition, results in the substitution Pro143 Ser in the third putative transmembrane domain of the adrenoleukodystrophy protein (ALDP) in an adult onset case. The second, a de novo C709T transition, results in a substitution Ser 108 Leu between the second and the third putative transmembrane segments, in a childhood case.lld:pubmed
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pubmed-article:10369742pubmed:copyrightInfoCopyright 1999 Academic Press.lld:pubmed
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pubmed-article:10369742pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:10369742pubmed:articleTitleTwo novel missense mutations causing adrenoleukodystrophy in Italian patients.lld:pubmed
pubmed-article:10369742pubmed:affiliationIst. Biologia e Genetica, Università di Verona, Italia.lld:pubmed
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