Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Transferrin isoelectrofocusing type 1 pattern"'
Autor:
Kellie Davis, Duncan Webster, Chris Smith, Sheryl Jackson, David Sinasac, Lorne Seargeant, Xing-Chang Wei, Patrick Ferreira, Julian Midgley, Yolanda Foster, Xueli Li, Miao He, Walla Al-Hertani
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 13, Iss C, Pp 55-63 (2017)
Congenital disorders of glycosylation (CDG) are a group of metabolic diseases resulting from defects in glycan synthesis or processing. The number of subgroups and their phenotypic spectrums continue to expand with most related to deficiencies of N-g
Externí odkaz:
https://doaj.org/article/d1627cb3e24a413c97327ac4fe3dbc0c
Autor:
Xing Chang Wei, David S. Sinasac, Kellie Davis, Duncan Webster, Patrick Ferreira, Yolanda Foster, Miao He, Julian P. Midgley, Walla Al-Hertani, Xueli Li, Sheryl Jackson, L.E. Seargeant, Christopher Smith
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 13, Iss C, Pp 55-63 (2017)
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports
Congenital disorders of glycosylation (CDG) are a group of metabolic diseases resulting from defects in glycan synthesis or processing. The number of subgroups and their phenotypic spectrums continue to expand with most related to deficiencies of N-g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f81557d000d25bfa6db9114563d50c3
https://doi.org/10.1016/j.ymgmr.2017.08.004
https://doi.org/10.1016/j.ymgmr.2017.08.004
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