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Miroslav P. Milev

Concordia University

17

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233

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The phenotype associated with variants in TANGO2 may be explained by a dual role of the protein in ER-to-Golgi transport and at the mitochondria.

2020 Journal of Inherited Metabolic Disease
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Publisher Correction: Characterization of three TRAPPC11 variants suggests a critical role for the extreme carboxy terminus of the protein.

2020 Scientific Reports
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TRAPPC11-Related Muscular Dystrophy with Hypoglycosylation of Alpha-Dystroglycan in Skeletal Muscle and Brain

2020
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Author response for "TRAPPC11 functions in autophagy by recruiting ATG2B-WIPI4/WDR45 to preautophagosomal membranes"

2019
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Characterization of three TRAPPC11 variants suggests a critical role for the extreme carboxy terminus of the protein

2019 Scientific Reports
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TRAPPopathies: An emerging set of disorders linked to variations in the genes encoding transport protein particle (TRAPP)‐associated proteins

2019 Traffic
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Bi-allelic mutations in TRAPPC2L result in a neurodevelopmental disorder and have an impact on RAB11 in fibroblasts

2018 Journal of Medical Genetics
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10 – Impacts of virus-mediated manipulation of host Dynein

2018
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TRAPPC11 and GOSR2 mutations associate with hypoglycosylation of α-dystroglycan and muscular dystrophy

2018 Skeletal Muscle
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Mutations in TRAPPC12 Manifest in Progressive Childhood Encephalopathy and Golgi Dysfunction

2017 American Journal of Human Genetics
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