Matches in DBpedia 2016-04 for { <http://doi.org/10.1007/s004310051009> ?p ?o }
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- s004310051009 date "Jan 1999".
- s004310051009 doi "10.1007/s004310051009".
- s004310051009 first1 "B".
- s004310051009 first10 "A".
- s004310051009 first2 "P".
- s004310051009 first3 "JC".
- s004310051009 first4 "V".
- s004310051009 first5 "D".
- s004310051009 first6 "A".
- s004310051009 first7 "D".
- s004310051009 first8 "JM".
- s004310051009 first9 "P".
- s004310051009 isCitedBy Neuropathy,_ataxia,_and_retinitis_pigmentosa.
- s004310051009 issue "1".
- s004310051009 journal "European journal of pediatrics".
- s004310051009 last1 "Parfait".
- s004310051009 last10 "Munnich".
- s004310051009 last2 "de Lonlay".
- s004310051009 last3 "von Kleist-Retzow".
- s004310051009 last4 "Cormier-Daire".
- s004310051009 last5 "Chrétien".
- s004310051009 last6 "Rötig".
- s004310051009 last7 "Rabier".
- s004310051009 last8 "Saudubray".
- s004310051009 last9 "Rustin".
- s004310051009 pages "55–8".
- s004310051009 pmid "9950309".
- s004310051009 title "The neurogenic weakness, ataxia and retinitis pigmentosa syndrome mtDNA mutation triggers muscle ATPase deficiency and hypocitrullinaemia.".
- s004310051009 volume "158".