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