Matches in DBpedia 2015-10 for { <http://doi.org/10.1034/j.1399-0004.2003.00138.x> ?p ?o }
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- j.1399-0004.2003.00138.x author "Devon RS".
- j.1399-0004.2003.00138.x author2 "Helm JR".
- j.1399-0004.2003.00138.x author3 "Rouleau GA".
- j.1399-0004.2003.00138.x displayAuthors "3".
- j.1399-0004.2003.00138.x doi "10.1034/j.1399-0004.2003.00138.x".
- j.1399-0004.2003.00138.x first4 "Y".
- j.1399-0004.2003.00138.x first5 "T".
- j.1399-0004.2003.00138.x first6 "D".
- j.1399-0004.2003.00138.x first7 "MR".
- j.1399-0004.2003.00138.x isCitedBy ALS2.
- j.1399-0004.2003.00138.x issue "3".
- j.1399-0004.2003.00138.x journal "Clin. Genet.".
- j.1399-0004.2003.00138.x last4 "Leitner".
- j.1399-0004.2003.00138.x last5 "Lerman-Sagie".
- j.1399-0004.2003.00138.x last6 "Lev".
- j.1399-0004.2003.00138.x last7 "Hayden".
- j.1399-0004.2003.00138.x nameListFormat "vanc".
- j.1399-0004.2003.00138.x pages "210–5".
- j.1399-0004.2003.00138.x pmid "12919135".
- j.1399-0004.2003.00138.x title "The first nonsense mutation in alsin results in a homogeneous phenotype of infantile-onset ascending spastic paralysis with bulbar involvement in two siblings".
- j.1399-0004.2003.00138.x volume "64".
- j.1399-0004.2003.00138.x year "2004".