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ESCO2 gene
Known as:
EFO2
, ESTABLISHMENT FACTOR ORTHOLOG 2
, ECO1, S. CEREVISIAE, HOMOLOG OF, 2
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National Institutes of Health
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Papers overview
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2020
2020
Roberts syndrome in an Indian patient with humeroradial synostosis, congenital elbow contractures and a novel homozygous splice variant in ESCO2
Pauline E Schneeberger
,
Shalini S Nayak
,
S. Fuchs
,
K. Kutsche
,
K. Girisha
American Journal of Medical Genetics. Part A
2020
Corpus ID: 221109396
Roberts syndrome (also known as Roberts‐SC phocomelia syndrome) is an autosomal recessive developmental disorder, characterized…
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2016
2016
The interaction between Esco2 and MCM complex protects Esco2 from proteasome-dependent degradation to establish cohesion
Shoin Tei
,
Masashi Minamino
,
Mai Ishibashi
,
Ryuichiro Nakato
,
M. Bando
,
K. Shirahige
2016
Corpus ID: 100433127
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