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CDC-Authored Genomics and Precision Health Publications Database|Home|Public Health Genomics and Precision Health Knowledge Base (PHGKB)

CDC-Authored Genomics and Precision Health Publications Database


Rare Diseases

Last data update: Dec 09, 2024. (Total: 6442 publications)
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Records 1-2 (of 2 Records)
Query Trace: Myotonic Dystrophy Type 1[original query]
Latent factors underlying the symptoms of adult-onset myotonic dystrophy type 1 during the clinical course
Zhang Y , Wallace B , Cai B , Johnson N , Ciafaloni E , Venkatesh YS , Westfield C , McDermott S .
Orphanet J Rare Dis 2024 19 (1) 409
Development of a genomic DNA reference material panel for myotonic dystrophy type 1 (DM1) genetic testing.
Kalman L , Tarleton J , Hitch M , Hegde M , Hjelm N , Berry-Kravis E , Zhou L , Hilbert JE , Luebbe EA , Moxley RT 3rd , Toji L .
J Mol Diagn 2013 15 (4) 518-25
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