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Statements

Subject Item
n2:RIV%2F61388971%3A_____%2F02%3A53020008%21RIV%2F2003%2FAV0%2FA53003%2FN
rdf:type
skos:Concept n17:Vysledek
dcterms:description
Friedreich ataxia (FRDA) is an autosomal recessive degenerative disease caused by a deficiency of frataxin, a conserved mitochondrial protein of unknown function. Friedreich ataxia (FRDA) is an autosomal recessive degenerative disease caused by a deficiency of frataxin, a conserved mitochondrial protein of unknown function.
dcterms:title
Assembly and iron-binding properties of human frataxin, the protein deficient in Friedreich ataxia. Assembly and iron-binding properties of human frataxin, the protein deficient in Friedreich ataxia.
skos:prefLabel
Assembly and iron-binding properties of human frataxin, the protein deficient in Friedreich ataxia. Assembly and iron-binding properties of human frataxin, the protein deficient in Friedreich ataxia.
skos:notation
RIV/61388971:_____/02:53020008!RIV/2003/AV0/A53003/N
n4:strany
217;227
n4:aktivita
n14:Z
n4:aktivity
Z(AV0Z5020903)
n4:cisloPeriodika
3
n4:dodaniDat
n13:2003
n4:domaciTvurceVysledku
n9:5791006
n4:druhVysledku
n8:J
n4:duvernostUdaju
n10:S
n4:entitaPredkladatele
n5:predkladatel
n4:idSjednocenehoVysledku
639040
n4:idVysledku
RIV/61388971:_____/02:53020008
n4:jazykVysledku
n16:eng
n4:klicovaSlova
assembly; human; frataxin
n4:klicoveSlovo
n11:assembly n11:frataxin n11:human
n4:kodStatuVydavatele
GB - Spojené království Velké Británie a Severního Irska
n4:kontrolniKodProRIV
[45F09A69531C]
n4:nazevZdroje
Human Molecular Genetics
n4:obor
n7:EE
n4:pocetDomacichTvurcuVysledku
1
n4:pocetTvurcuVysledku
4
n4:pocetUcastnikuAkce
0
n4:pocetZahranicnichUcastnikuAkce
0
n4:rokUplatneniVysledku
n13:2002
n4:svazekPeriodika
11
n4:tvurceVysledku
Isaya, G. ONeill, H. Benada, Oldřich Cavadini, P.
n4:zamer
n15:AV0Z5020903
s:issn
0964-6906
s:numberOfPages
11