Rat neurological disease creeping is caused by a mutation in the reelin gene
about
Prioritizing the development of mouse models for childhood brain disordersGenetic profiling of two phenotypically distinct outbred rats derived from a colony of the Zucker fatty rats maintained at Tokyo Medical University.Identification of a 31-bp deletion in the RELN gene causing lissencephaly with cerebellar hypoplasia in sheep.Reelin in the Years: Controlling Neuronal Migration and Maturation in the Mammalian Brain
P2860
Rat neurological disease creeping is caused by a mutation in the reelin gene
description
2003 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2003
@ast
im April 2003 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2003/04/10)
@sk
vědecký článek publikovaný v roce 2003
@cs
wetenschappelijk artikel (gepubliceerd op 2003/04/10)
@nl
наукова стаття, опублікована у квітні 2003
@uk
مقالة علمية (نشرت في 10-4-2003)
@ar
name
Rat neurological disease creeping is caused by a mutation in the reelin gene
@ast
Rat neurological disease creeping is caused by a mutation in the reelin gene
@en
Rat neurological disease creeping is caused by a mutation in the reelin gene
@nl
type
label
Rat neurological disease creeping is caused by a mutation in the reelin gene
@ast
Rat neurological disease creeping is caused by a mutation in the reelin gene
@en
Rat neurological disease creeping is caused by a mutation in the reelin gene
@nl
prefLabel
Rat neurological disease creeping is caused by a mutation in the reelin gene
@ast
Rat neurological disease creeping is caused by a mutation in the reelin gene
@en
Rat neurological disease creeping is caused by a mutation in the reelin gene
@nl
P2093
P1476
Rat neurological disease creeping is caused by a mutation in the reelin gene
@en
P2093
He-Yao Wang
Kajuro Komeda
Kazuki Yasuda
Ken Kojima
Masanori Fuse
Misako Namae
Norihide Yokoi
Susumu Seino
Tadao Serikawa
P356
10.1016/S0169-328X(02)00650-2
P577
2003-04-10T00:00:00Z