| 1 | ALS2, IAHSP
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| Novel homozygous ALS2 nonsense mutation (p.Gln715X) in sibs with infantile-onset ascending spastic paralysis: the first cases from northwestern Europe.
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| Verschuuren-Bemelmans CC, Winter P, Sival DA, Elting JW, Brouwer OF, Müller U.
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| Eur J Hum Genet 16(11):1407-11. Epub 2008 Jun 4.
2008
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| 2 | ALS2, PLSJ, IAHSP
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| A novel somatodendritic marker defined by a peptide derived from the ALS2 protein.
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| Bros V, Shemilt SJ, Cooper JD, Skaper SD, Leigh PN, Gallo JM.
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| Neuroreport 15(14):2155-9. 2004
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| 3 | ALS2, IAHSP
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| Infantile ascending hereditary spastic paralysis (IAHSP): clinical features in 11 families.
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| Lesca G, Eymard-Pierre E, Santorelli FM, Cusmai R, Di Capua M, Valente EM, Attia-Sobol J, Plauchu H, Leuzzi V, Ponzone A, Boespflug-Tanguy O, Bertini E.
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| Neurology 60(4):674-82. 2003
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| 4 | ALS2, IAHSP
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| Infantile-onset ascending hereditary spastic paralysis is associated with mutations in the alsin gene.
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| Eymard-Pierre E, Lesca G, Dollet S, Santorelli FM, di Capua M, Bertini E, Boespflug-Tanguy O.
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| Am J Hum Genet 71(3):518-27. Epub 2002 Jul 26. 2002
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