A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip (Q34093285)
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English | A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip |
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A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip (English)
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Ludwig Lehle
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Nina Rind
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Christian Körner
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Verena Schmeiser
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Christian Thiel
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Birgit Absmanner
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Jürgen Lübbehusen
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Julia Hocks
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Neophytos Apeshiotis
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Ekkehard Wilichowski
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15 January 2010
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19
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1413-1424
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