2024-03-29T00:38:30Z
http://repoint.unil.ch/oaiprovider/
oai:serval.unil.ch:BIB_29D795794213
2024-03-23T02:04:41Z
serval:BIB_29D795794213
Bi-allelic Variants in DYNC1I2 Cause Syndromic Microcephaly with Intellectual Disability, Cerebral Malformations, and Dysmorphic Facial Features.
10.1016/j.ajhg.2019.04.002
000470240000005
31079899
Ansar
M.
author
Ullah
F.
author
Paracha
S.A.
author
Adams
D.J.
author
Lai
A.
author
Pais
L.
author
Iwaszkiewicz
J.
author
Millan
F.
author
Sarwar
M.T.
author
Agha
Z.
author
Shah
S.F.
author
Qaisar
A.A.
author
Falconnet
E.
author
Zoete
V.
author
Ranza
E.
author
Makrythanasis
P.
author
Santoni
F.A.
author
Ahmed
J.
author
Katsanis
N.
author
Walsh
C.
author
Davis
E.E.
author
Antonarakis
S.E.
author
article
2019-06-06
American journal of human genetics
1537-6605
0002-9297
journal
104
6
1073-1087
Dync1i2
apoptosis
autosomal recessive
developmental delay
dynein
dysmorphic facial features
intellectual disability
microcephaly
mitotic spindle
zebrafish
DYNC1I2
eng
60_published
peer-reviewed
Publication types: Journal Article
Publication Status: ppublish