Biallelic variants in CRIPT cause a Rothmund-Thomson-like syndrome with increased cellular senescence
Author:
Funder
European Organization for Nuclear Research
European Research Council
Deutsche Forschungsgemeinschaft
Bundesministerium für Bildung und Forschung
BMBF Berlin
Publisher
Elsevier BV
Subject
Genetics (clinical)
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4. An hitherto undescribed familial disease;Thomson;Br J Dermatol,1923
5. Rothmund-Thomson syndrome, Klippel-Feil syndrome, and osteosarcoma;Gelaw;Skeletal Radiol,2004
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