A compound heterozygous mutation in DPAGT1 results in a congenital disorder of glycosylation with a relatively mild phenotype
scientific article published on 19 December 2012
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author: Zafar Iqbal, Lisenka Vissers, Christian Gilissen, Joris A Veltman, Hans van Bokhoven, Arjan P M de Brouwer, Dirk J Lefeber, Tjitske Kleefstra, Muhammad Yasir Zahoor, Sheikh Riazuddin, Attia Razzaq
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