Retraction
Identification of seven novel mutations in ABCD1 by a DHPLC‐based assay in Italian patients with X‐linked adrenoleukodystrophy
Paper Information
Record ID:
24339
Author(s):
Journal:
Human Mutation
(
Wiley
)
Publication Date:
January 10, 2005
Retraction Date:
August 25, 2020
(5.2 years years ago)
Subjects:
Country:
🇮🇹 ItalyArticle Type:
Publisher:
Wiley
Open Access:
Yes
DOI:
PubMed ID:
Retraction PubMed ID:
Retraction Details
Citations (13)
13
Total Citations3
Post-Retraction(23.1%)
10
Pre-Retraction0
Same DayPost-Retraction Citation Analysis
0
Within 30 days
2
Within 1 year
0
After 2+ years
531
Days since retraction (latest)
Identification of Two Novel Mutations of ABCD1 Gene in Pedigrees with X-Linked Adrenoleukodystrophy and Review of the Literature
Bingzi Dong, Wenshan Lv, Lili Xu et al. (9 authors)
International Journal of Endocrinology
Open Access
Published: Feb 2022
10 citations
10 citations
531 days after retraction
A Large Family with p.Arg554His Mutation in ABCD1: Clinical Features and Genotype/Phenotype Correlation in Female Carriers
Rosa Campopiano, Cinzia Femiano, Maria Antonietta Chiaravalloti et al. (15 authors)
Genes
Open Access
Published: May 2021
7 citations
7 citations
267 days after retraction
Sex Chromosome-Linked Diseases
Haibo Li, Lulu Yan, Yuxin Zhang et al. (7 authors)
Comprehensive gynecology and obstetrics
Published: Dec 2020
102 days after retraction
Late adult-onset adrenomyeloneuropathy evolving with atypical severe frontal lobe syndrome: Importance of neuroimaging
Clemente Dato, G Capaldo, Chiara Terracciano et al. (10 authors)
Radiology Case Reports
Open Access
Published: Dec 2018
4 citations
4 citations
629 days before retraction
Prenatal diagnosis of X‐linked adrenoleukodystrophy associated with isolated pericardial effusion
Giovanna Traficante, Roberto Biagiotti, Elena Andreucci et al. (7 authors)
Clinical Case Reports
Open Access
Published: Jun 2015
3 citations
3 citations
1902 days before retraction
Discordant diagnoses obtained by different approaches in antithrombin mutation analysis
Søren Feddersen, Mads Nybo
Clinical Biochemistry
Published: Jun 2014
2 citations
2 citations
2258 days before retraction
Novel exon nucleotide deletion causes adrenoleukodystrophy in a Brazilian family
Eugênia Ribeiro Valadares, Amelia Trindade, Luiz Roberto de Oliveira et al. (10 authors)
Genetics and Molecular Research
Open Access
Published: Jan 2011
4 citations
4 citations
3524 days before retraction
Denaturing HPLC for Mutation Screening
Mike Mitchell, Jacqueline A. Cutler
Methods in molecular biology
Published: Oct 2010
4 citations
4 citations
3612 days before retraction
Linking mutated primary structure of adrenoleukodystrophy protein with X-linked adrenoleukodystrophy
Shaomin Yan, Guang Wu
Computer Methods in Biomechanics & Biomedical Engineering
Published: Jan 2010
3 citations
3 citations
3876 days before retraction
A new method avoids interference of ABCD1 pseudogenes in molecular diagnosis of X-linked adrenoleukodystrophy
Longfeng Ke, Lianghu Huang, Zhihong Wang et al. (7 authors)
Academic Journal of Second Military Medical University
Published: Jun 2009
1 citation
1 citation
4095 days before retraction
Adrenoleukodystrophy: Molecular, Metabolic, Pathologic, and Therapeutic Aspects
Miguel Á. Contreras, Inderjit Singh
Springer eBooks
Published: Sep 2008
2 citations
2 citations
4362 days before retraction
Mutational Analyses of Taiwanese Kindred With X-linked Adrenoleukodystrophy
Hou‐Chang Chiu, Jao‐Shwann Liang, Jinn‐Shyan Wang et al. (4 authors)
Pediatric Neurology
Published: Sep 2006
10 citations
10 citations
5086 days before retraction
<i>Retracted</i> : Identification of seven novel mutations in ABCD1 by a DHPLC‐based assay in Italian patients with X‐linked adrenoleukodystrophy
Giorgia Montagna, A. De Biase, Marco Cappa et al. (12 authors)
Human Mutation
Open Access
Published: Jan 2005
13 citations
13 citations
5706 days before retraction
Quick Stats
Total Citations:
13
Years Since Retraction:
5.2 years
Open Access:
Yes
Last Checked:
Jul 24, 2025