Associated Papers
Genetic dynamics in untreated CLL patients with either stable or progressive disease: a longitudinal study.
Ramassone A et al.
Journal of Hematology & Oncology, 2019
31744508 (PubMed )
Supplement: 13045_2019_802_MOESM7_ESM.xlsx › Foglio1
Mutational analysis of GJB1, MPZ, PMP22, EGR2, and LITAF/SIMPLE in Serbian Charcot-Marie-Tooth patients.
Keckarevic-Markovic M et al.
Journal of the Peripheral Nervous System : Jpns, 2009
Novel EGR2 mutation R359Q is associated with CMT type 1 and progressive scoliosis.
Mikesová E et al.
Neuromuscular Disorders : Nmd, 2005
Frequency of mutations in the early growth response 2 gene associated with peripheral demyelinating neuropathies.
Vandenberghe N et al.
Journal of Medical Genetics, 2002
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