MECP2, a gene associated with Rett syndrome in humans, shows conserved coding regions, independent Alu insertions, and a novel transcript across primate evolution
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MECP2, a gene associated with Rett syndrome in humans, shows conserved coding regions, independent Alu insertions, and a novel transcript across primate evolution
description
2015 nî lūn-bûn
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2015年の論文
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2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
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2015年论文
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2015年论文
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name
MECP2, a gene associated with ...... cript across primate evolution
@ast
MECP2, a gene associated with ...... cript across primate evolution
@en
type
label
MECP2, a gene associated with ...... cript across primate evolution
@ast
MECP2, a gene associated with ...... cript across primate evolution
@en
prefLabel
MECP2, a gene associated with ...... cript across primate evolution
@ast
MECP2, a gene associated with ...... cript across primate evolution
@en
P2093
P2860
P1433
P1476
MECP2, a gene associated with ...... cript across primate evolution
@en
P2093
Albert Nobre Menezes
Alcides Pissinatti
Héctor N Seuánez
Maria Carolina Viana
Miguel Angelo M Moreira
P2860
P2888
P356
10.1186/S12863-015-0240-X
P577
2015-07-07T00:00:00Z
P5875
P6179
1002457386