| 1 | IDS, IDSP1
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| Homologous nonallelic recombinations between the iduronate-sulfatase gene and pseudogene cause various intragenic deletions and inversions in patients with mucopolysaccharidosis type II.
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| Bunge S, Rathmann M, Steglich C, Bondeson ML, Tylki-Szymanska A, Popowska E, Gal A.
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| Eur J Hum Genet 6(5):492-500. 1998
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| 2 | IDS, IDSP1, IDSCR
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| Molecular and phenotypic variation in patients with severe Hunter syndrome.
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| Timms KM, et al.
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| Hum Mol Genet 6 : 479-486. 1997
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| 3 | IDS, IDSP1
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| Double-strand breaks may initiate the inversion mutation causing the Hunter syndrome.
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| Lagerstedt K, et al.
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| Hum Mol Genet 6 : 627-633. 1997
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| 4 | IDS, IDSP1, IDSCR
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| Two distinct deletions in the IDS gene and the gene W: a novel type of mutation associated with the Hunter syndrome.
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| Karsten SL, Lagerstedt K, Carlberg BM, Kleijer WJ, Zaremba J, Van Diggelen OP, Czartoryska B, Pettersson U, Bondeson ML.
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| Genomics 43(2):123-9. 1997
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| 5 | IDS, IDSP1
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| IDS gene-pseudogene exchange responsible for an intragenic deletion in aHunter patient.
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| Birot AM, et al.
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| Hum Mutat 8 : 44-50. 1996
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| 6 | IDSP1
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| Presence of an IDS-related locus (IDS2) in Xq28 complicates the mutational analysis of Hunter syndrome.
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| Bondeson ML, et al.
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| Eur J Hum Genet 3 : 219-227. 1995
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| 7 | IDS, IDSP1, MPS2
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| Inversion of the IDS gene resulting from recombination with IDS-related sequences is a common cause of the Hunter syndrome.
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| Bondeson ML, et al.
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| Hum Mol Genet 4 : 615-621. 1995
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| 8 | IDSP1
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| Evidence for an iduronate-sulfatase pseudogene near the functional Hunter syndrome gene in Xq27.3-q28.
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| Rathmann M, et al.
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| Hum Genet 95 : 34-38. 1995
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| 9 | IDS, IDSCR, IDSP1
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| 130 kb of DNA sequence reveals two new genes and a regional duplication distal to the human iduronate-2-sulfate sulfatase locus.
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| Timms KM, Lu F, Shen Y, Pierson CA, Muzny DM, Gu Y, Nelson DL, Gibbs RA.
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| Genome Res 5(1):71-8. 1995
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