Ontology highlight
ABSTRACT:
SUBMITTER: Wang Y
PROVIDER: S-EPMC5773358 | biostudies-literature | 2018 Mar
REPOSITORIES: biostudies-literature
Wang Youjin Y Pfeiffer Ruth M RM Alsaggaf Rotana R Meeraus Wilhelmine W Gage Julia C JC Anderson Lesley A LA Bremer Renée C RC Nikolenko Nikoletta N Lochmuller Hanns H Greene Mark H MH Gadalla Shahinaz M SM
International journal of cancer 20171120 6
Myotonic dystrophy type 1 (DM1) is an inherited multisystem neuromuscular disorder caused by a CTG trinucleotide repeat expansion in the DMPK gene. Recent evidence documents that DM1 patients have an increased risk of certain cancers, but whether skin cancer risks are elevated is unclear. Using the U.K. Clinical Practice Research Datalink (CPRD), we identified 1,061 DM1 patients and 15,119 DM1-free individuals matched on gender, birth year (±2 years), attending practice and registration year (±1 ...[more]