Literature DB >> 10980539

Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations.

M G Lira1, M Mottes, P F Pignatti, I Medica, G Uziel, M Cappa, E Bertini, N Rizzuto, A Salviati.   

Abstract

The study describes the mutations causing adrenoleukodystrophy in seven Italian families. Four missense mutations leading to amino acid substitutions, two frameshift mutations leading to a premature termination signal, and a splicing mutation were identified. Mutations 2014C>T (P543L), 2053A>G (Q556A), 673-674insCC, and 1874+1G>A are described for the first time in this report. Mutations 1638C>T (R418W), 1588G>A(R401Q), and 1801-1802delAG are already known to be link to ALD. Copyright 2000 Wiley-Liss, Inc.

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Year:  2000        PMID: 10980539     DOI: 10.1002/1098-1004(200009)16:3<271::AID-HUMU15>3.0.CO;2-D

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  2 in total

1.  Adrenomyeloneuropathy in patients with 'Addison's disease': genetic case analysis.

Authors:  Sagarika Mukherjee; Elizabeth Newby; John N Harvey
Journal:  J R Soc Med       Date:  2006-05       Impact factor: 18.000

2.  Identification of Two Novel Mutations of ABCD1 Gene in Pedigrees with X-Linked Adrenoleukodystrophy and Review of the Literature.

Authors:  Bingzi Dong; Wenshan Lv; Lili Xu; Yuhang Zhao; Xiaofang Sun; Zhongchao Wang; Bingfei Cheng; Zhengju Fu; Yangang Wang
Journal:  Int J Endocrinol       Date:  2022-02-07       Impact factor: 2.803

  2 in total

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