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Gene symbol: MECP2. Disease: Rett syndrome
D Zahorakova, V Juttnerova, J Zeman, P Martasek
Language English Country Germany
NLK
ProQuest Central
from 2000-01-01 to 1 year ago
Medline Complete (EBSCOhost)
from 2000-01-01 to 1 year ago
Health & Medicine (ProQuest)
from 2000-01-01 to 1 year ago
Public Health Database (ProQuest)
from 2000-01-01 to 1 year ago
- MeSH
- Gene Deletion MeSH
- Codon genetics MeSH
- Humans MeSH
- Frameshift Mutation MeSH
- Methyl-CpG-Binding Protein 2 genetics MeSH
- Rett Syndrome genetics MeSH
- Codon, Terminator MeSH
- Check Tag
- Humans MeSH
- 000
- 01175naa 2200325 a 4500
- 001
- bmc11005106
- 003
- CZ-PrNML
- 005
- 20140203084119.0
- 008
- 110311s2008 gw e eng||
- 009
- AR
- 040 __
- $a ABA008 $b cze $c ABA008 $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a gw
- 100 1_
- $a Záhoráková, Daniela $7 xx0074483
- 245 10
- $a Gene symbol: MECP2. Disease: Rett syndrome / $c D Zahorakova, V Juttnerova, J Zeman, P Martasek
- 314 __
- $a First School of Medicine Charles University, Department of Pediatrics, Ke Karlovu, 2, 12808 Prague, Czech Republic. zahorakova@gmail.com
- 650 _2
- $a kodon $x genetika $7 D003062
- 650 _2
- $a terminační kodon $7 D018388
- 650 _2
- $a posunová mutace $7 D016368
- 650 _2
- $a delece genu $7 D017353
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a protein 2 vázající methyl-CpG $x genetika $7 D051783
- 650 _2
- $a Rettův syndrom $x genetika $7 D015518
- 700 1_
- $a Jüttnerová, Věra $7 xx0105883
- 700 1_
- $a Zeman, Jiří, $d 1950- $7 skuk0001517
- 700 1_
- $a Martásek, Pavel, $d 1952- $7 xx0077949
- 773 0_
- $t Human Genetics $w MED00002074 $g Roč. 124, č. 3 (2008), s. 315
- 910 __
- $a ABA008 $b x $y 1 $z 0
- 990 __
- $a 20110414094550 $b ABA008
- 991 __
- $a 20140203084857 $b ABA008
- 999 __
- $a ok $b bmc $g 832953 $s 697156
- BAS __
- $a 3
- BMC __
- $a 2008 $b 124 $c 3 $d 315 $m Human genetics $n Hum. genet. $x MED00002074
- LZP __
- $a 2011-4B/vtme