Associated Papers
Whole-Exome Sequencing Revealed New Candidate Genes for Human Dilated Cardiomyopathy.
D'Agostino Y et al.
Diagnostics (basel, Switzerland), 2022
36292100 (PubMed )
Supplement: diagnostics-12-02411-s001.zip › Supplementary_table_S3.xlsx › Foglio1
A novel mutation in PRDM5 in brittle cornea syndrome.
Aldahmesh MA et al.
Clinical Genetics, 2012
Clinical and Genetic Analysis of A Father-Son Duo with Monomelic Amyotrophy: Case Report.
Khurana S et al.
Annals of Indian Academy of Neurology, 0
Select a paper to view details