| Literature DB >> 10980539 |
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.Entities:
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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