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4
results
Myotonic Dystrophy Type 1 - GeneReviews® - NCBI Bookshelf
... Locus Protein Locus-Specific Databases HGMD ClinVar DMPK
19q13 .32
Myotonin-protein kinase DMPK database DMPK DMPK Data ...
Most Recent PubMed Articles
Phenotypic expression of
19q13.32
microdeletions
: Report of a new patient and
review
of the literature.
19q13.32
microdeletion
syndrome: three new cases.
Lack of association between genetic variants in the
19q13.32
region and CHD risk in the Algerian
population: a population
-based nested case-
control
study.
More articles »
