127 related articles for article (PubMed ID: 21488311)
1. Novel human pathological mutations. Gene symbol: ABCD1. Disease: X-linked adrenoleukodystrophy.
Amorosi CA; Treslova H; Dodelson de Kremer R; Coll MJ; Dvoráková L; Oller Ramírez AM
Hum Genet; 2010 Apr; 127(4):486. PubMed ID: 21488311
[No Abstract] [Full Text] [Related]
2. Novel human pathological mutations. Gene symbol: ABCD1. Disease: X-linked adrenoleukodystrophy.
Amorosi CA; Treslova H; Dodelson de Kremer R; Coll MJ; Dvoráková L; Oller Ramírez AM
Hum Genet; 2010 Apr; 127(4):486-7. PubMed ID: 21488264
[No Abstract] [Full Text] [Related]
3. Novel human pathological mutations. Gene symbol: ABCD1. Disease: X-linked adrenoleukodystrophy.
Amorosi CA; Treslova H; Dodelson de Kremer R; Coll MJ; Dvoráková L; Oller Ramírez AM
Hum Genet; 2010 Apr; 127(4):486. PubMed ID: 21488262
[No Abstract] [Full Text] [Related]
4. Novel human pathological mutations. Gene symbol: ABCD1. Disease: Adrenoleukodystrophy.
Shukla P; Gupta N; Kabra M; Ghosh M; Gulati S; Kalra V
Hum Genet; 2009 Aug; 126(2):335-6. PubMed ID: 19694007
[No Abstract] [Full Text] [Related]
5. Gene symbol: ABCD1. Disease: Adrenoleukodystrophy.
Shukla P
Hum Genet; 2008 Oct; 124(3):311. PubMed ID: 18846653
[No Abstract] [Full Text] [Related]
6. Gene symbol: ABCD1. Disease: Adrenoleukodystrophy.
Shukla P
Hum Genet; 2008 Oct; 124(3):312. PubMed ID: 18846655
[No Abstract] [Full Text] [Related]
7. Novel human pathological mutations. Gene symbol: ABCD1. Disease: Adrenoleukodystrophy.
Kumar N; Taneja KK; Kalra V; Behari M; Aneja S; Bansal SK
Hum Genet; 2009 Aug; 126(2):344. PubMed ID: 19694033
[No Abstract] [Full Text] [Related]
8. [X-linked adrenoleukodystrophy ABCD1 gene mutation analysis in China].
Pan H; Xiong H; Zhang YH; Wu Y; Bao XH; Jiang YW; Wu XR
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Feb; 21(1):1-4. PubMed ID: 14767898
[TBL] [Abstract][Full Text] [Related]
9. Three novel variants in X-linked adrenoleukodystrophy.
Shukla P; Gupta N; Kabra M; Ghosh M; Sharma R; Gupta AK; Gulati S; Kalra V
J Child Neurol; 2009 Jul; 24(7):857-60. PubMed ID: 19406751
[TBL] [Abstract][Full Text] [Related]
10. A novel mutation in the ABCD1 gene of a Moroccan patient with X-linked adrenoleukodystrophy: case report.
Karkar A; Barakat A; Bakhchane A; Fettah H; Slassi I; Dorboz I; Boespflug-Tanguy O; Nadifi S
BMC Neurol; 2015 Nov; 15():244. PubMed ID: 26607867
[TBL] [Abstract][Full Text] [Related]
11. Gene symbol: ABCD1. Disease: Adrenoleukodystrophy.
Shukla P
Hum Genet; 2008 Oct; 124(3):312. PubMed ID: 18846654
[No Abstract] [Full Text] [Related]
12. Mutational analyses on X-linked adrenoleukodystrophy reveal a novel cryptic splicing and three missense mutations in the ABCD1 gene.
Hung KL; Wang JS; Keng WT; Chen HJ; Liang JS; Ngu LH; Lu JF
Pediatr Neurol; 2013 Sep; 49(3):185-90. PubMed ID: 23835273
[TBL] [Abstract][Full Text] [Related]
13. Gene symbol: ABCD1.
Dvoráková L; Carrero-Valenzuela RD; Antelo T; Fagalde J; Merched D
Hum Genet; 2007 Apr; 121(2):288. PubMed ID: 17598227
[No Abstract] [Full Text] [Related]
14. Gene symbol: ABCD1.
Dvorakova L; Myskova H; Carrero-Valenzuela RD; Antelo T; Fagalde J; Merched D
Hum Genet; 2007 Apr; 121(2):287. PubMed ID: 17598197
[No Abstract] [Full Text] [Related]
15. Splicing defects in ABCD1 gene leading to both exon skipping and partial intron retention in X-linked adrenoleukodystrophy Tunisian patient.
Kallabi F; Hadj Salem I; Ben Chehida A; Ben Salah G; Ben Turkia H; Tebib N; Keskes L; Kamoun H
Neurosci Res; 2015 Aug; 97():7-12. PubMed ID: 25835712
[TBL] [Abstract][Full Text] [Related]
16. Mutations in the adrenoleukodystrophy gene.
Dodd A; Rowland SA; Hawkes SL; Kennedy MA; Love DR
Hum Mutat; 1997; 9(6):500-11. PubMed ID: 9195223
[TBL] [Abstract][Full Text] [Related]
17. Novel exon nucleotide deletion causes adrenoleukodystrophy in a Brazilian family.
Valadares ER; Trindade AL; Oliveira LR; Arantes RR; Daker MV; Viana BM; Haase VG; Jardim LB; Lopes GC; Godard AL
Genet Mol Res; 2011 Jan; 10(1):65-74. PubMed ID: 21264817
[TBL] [Abstract][Full Text] [Related]
18. A de-novo large deletion of 2.8 kb produced in the ABCD1 gene causing adrenoleukodystrophy disease.
Kallabi F; Ben Salah G; Ben Chehida A; Tabebi M; Felhi R; Ben Turkia H; Tebib N; Keskes L; Kamoun H
Biochem Cell Biol; 2016 Jun; 94(3):265-9. PubMed ID: 27248780
[TBL] [Abstract][Full Text] [Related]
19. Phenotypic variability in a Tunisian family with X-linked adrenoleukodystrophy caused by the p.Gln316Pro novel mutation.
Kallabi F; Ellouz E; Tabebi M; Ben Salah G; Kaabechi N; Keskes L; Triki C; Kamoun H
Clin Chim Acta; 2016 Jan; 453():141-6. PubMed ID: 26686776
[TBL] [Abstract][Full Text] [Related]
20. Oligosymptomatic adrenomyeloneuropathy due to a novel mutation in the ABCD1 start codon.
Dunkl V; Rau I; Wunderlich G; Fink GR; Lehmann HC
J Neurol Sci; 2016 Aug; 367():81-2. PubMed ID: 27423567
[No Abstract] [Full Text] [Related]
[Next] [New Search]
