Publications by authors named "Ieva Micule"

5Publications

Collagen VI-related limb-girdle syndrome caused by frequent mutation in COL6A3 gene with conflicting reports of pathogenicity.

Neuromuscul Disord 2020 06 18;30(6):483-491. Epub 2020 Apr 18.

Latvian Biomedical Research and Study Centre, Ratsupites 1, Riga LV-1067, Latvia; Medical Genetics department, CHUQ, 2705 Blvd Laurier, Quebec City, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.nmd.2020.03.010DOI Listing
June 2020

Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance.

Hum Mol Genet 2014 Jun 8;23(11):2888-900. Epub 2014 Jan 8.

Sektion für Funktionelle Genetik am Institut für Humangenetik, Universität zu Lübeck, Lübeck 23538, Germany.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/hmg/ddu002DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4014191PMC
June 2014

Dupuytren's Contracture Cosegregation with Limb-Girdle Muscle Dystrophy.

Case Rep Neurol Med 2013 19;2013:254950. Epub 2013 Aug 19.

Latvian Biomedical Research and Study Centre, Ratsupites Street 1, Riga 1067, Latvia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1155/2013/254950DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3760302PMC
September 2013