Hmn (hereditary Motor Neuropathy) Proximal Type I: Disease Bioinformatics
Research of Hmn (hereditary Motor Neuropathy) Proximal Type I has been linked to Muscular Atrophy, Atrophy, Spinal Muscular Atrophy, Spinal Muscular Atrophies Of Childhood, Neuromuscular Diseases. The study of Hmn (hereditary Motor Neuropathy) Proximal Type I has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Hmn (hereditary Motor Neuropathy) Proximal Type I include Pathogenesis, Cell Death, Muscle Atrophy, Innervation, Programmed Cell Death. These pathways complement our catalog of research reagents for the study of Hmn (hereditary Motor Neuropathy) Proximal Type I including antibodies and ELISA kits against MOTOR NEURON DEGENERATION, BCL2, BCL2L1, BDNF, DES.
Top Research Reagents
We have 3215 products for the study of Hmn (hereditary Motor Neuropathy) Proximal Type I that can be applied to Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
Hmn (hereditary Motor Neuropathy) Proximal Type I is also known as Infantile Muscular Atrophies, Infantile Muscular Atrophy, Infantile Spinal Muscular Atrophy, Severe Infantile Spinal Muscular Atrophy, Spinal Muscular Atrophy 1.