Associated Papers
Characterization of rare germline variants in familial multiple myeloma.
Catalano C et al.
Blood Cancer Journal, 2021
33583942 (PubMed )
Supplement: 41408_2021_422_MOESM1_ESM.pdf
Exome sequencing identifies titin mutations causing hereditary myopathy with early respiratory failure (HMERF) in families of diverse ethnic origins.
Toro C et al.
Bmc Neurology, 2013
Select a paper to view details