Matches in DBpedia 2016-04 for { <http://doi.org/10.1007/s004390000432> ?p ?o }
Showing triples 1 to 24 of
24
with 100 triples per page.
- s004390000432 author "Santer R".
- s004390000432 author2 "Kinner M".
- s004390000432 author3 "Passarge M".
- s004390000432 displayAuthors "3".
- s004390000432 doi "10.1007/s004390000432".
- s004390000432 first4 "Reinhard".
- s004390000432 first5 "Ertan".
- s004390000432 first6 "Thomas".
- s004390000432 first7 "J�Rgen".
- s004390000432 first8 "Marie".
- s004390000432 isCitedBy GLUDP5.
- s004390000432 issue "1".
- s004390000432 journal "Hum. Genet.".
- s004390000432 last4 "Schneppenheim".
- s004390000432 last5 "Mayatepek".
- s004390000432 last6 "Meissner".
- s004390000432 last7 "Schaub".
- s004390000432 last8 "Passarge".
- s004390000432 nameListFormat "vanc".
- s004390000432 pages "66–71".
- s004390000432 pmid "11214910".
- s004390000432 title "Novel missense mutations outside the allosteric domain of glutamate dehydrogenase are prevalent in European patients with the congenital hyperinsulinism-hyperammonemia syndrome".
- s004390000432 volume "108".
- s004390000432 year "2001".