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Molecular Genetics and Metabolism. 2015; doi:10.1016/j.ymgme.2015.01.014. Metachromatic leukodystrophy. Merck Manual Professional Version. https://www ...
To establish a repository of DNA samples collected prospectively from patients with inherited myopathies of unknown molecular and/or biochemical defect. To ...
Biochimica et Biophysica Acta (BBA) Molecular Basis of Disease. 2016;1862:545. Receive Mayo Clinic news in your inbox. Sign up. Related Content.
Small molecule receptor tyrosine kinase inhibitor (TKI) therapy ... Note: Anticoagulation with therapeutic doses of low molecular weight heparin ...
The purpose of this study is to confirm detection of the H3K27M mutation in patient biofluids (CSF, blood, urine, saliva) and uncover the molecular histone ...
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