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oai:serval.unil.ch:BIB_32007FA54964
2024-03-23T02:08:05Z
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Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1
10.1086/344781
000179586800022
12434312
Dgany
O.
author
Avidan
N.
author
Delaunay
J.
author
Krasnov
T.
author
Shalmon
L.
author
Shalev
H.
author
Eidelitz-Markus
T.
author
Kapelushnik
J.
author
Cattan
D.
author
Pariente
A.
author
Tulliez
M.
author
Cretien
A.
author
Schischmanoff
P. O.
author
Iolascon
A.
author
Fibach
E.
author
Koren
A.
author
Rossler
J.
author
Le Merrer
M.
author
Yaniv
I.
author
Zaizov
R.
author
Ben-Asher
E.
author
Olender
T.
author
Lancet
D.
author
Beckmann
J. S.
author
Tamary
H.
author
article
2002-12
American Journal of Human Genetics
0002-9297
journal
71
6
1467-74
Amino Acid Sequence
Anemia, Dyserythropoietic, Congenital/*genetics
Base Sequence
Chromosomes, Human, Pair 15/genetics
Consanguinity
Erythropoiesis
Exons/genetics
Female
Glycoproteins/chemistry/*genetics
Humans
Israel
Male
Molecular Sequence Data
Mutation/*genetics
Pedigree
Phenotype
Protein Structure, Tertiary
RNA, Messenger/genetics/metabolism
Sequence Alignment
60_published
true
Journal Article
Research Support, Non-U.S. Gov't --- Old month value: Dec