Niemann-Pick disease type C. The diagram represents subtypes and
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Figure 1 from Linkage of Niemann-Pick disease type C to human chromosome 18.
Elevation of plasma lysosphingomyelin-509 and urinary bile acid metabolite in Niemann-Pick disease type C-affected individuals - Top Articles selected by the Editor - Molecular Genetics and Metabolism Reports - Journal - Elsevier
Determinants, maintenance, and function of organellar pH
Cellular Adaptations and Accumulations Flashcards
At a glance: the largest Niemann-Pick type C1 cohort with 602 patients diagnosed over 15 years
N-Substituted l-Iminosugars for the Treatment of Sanfilippo Type B Syndrome
Consensus clinical management guidelines for acid sphingomyelinase deficiency (Niemann–Pick disease types A, B and A/B), Orphanet Journal of Rare Diseases
Health insurance literacy and health services access barriers in Niemann–Pick disease: the patient and caregiver voice, Orphanet Journal of Rare Diseases
Resistance to hepatitis C virus: potential genetic and immunological determinants - The Lancet Infectious Diseases
Niemann–Pick type C disease: cellular pathology and pharmacotherapy - Wheeler - 2020 - Journal of Neurochemistry - Wiley Online Library
Niemann–Pick disease - Wikipedia
Niemann-Pick disease type C. The diagram represents subtypes and onset
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