Published in
BioMed Central, BMC Medical Genetics, 1(19), 2018
DOI: 10.1186/s12881-018-0617-6
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Mosaicism of the UDP-Galactose transporter SLC35A2 in a female causing a congenital disorder of glycosylation: a case report
Journal article published in 2018 by
Kristen Westenfield,
Kyriakie Sarafoglou,
Laura C. Speltz,
Elizabeth I. Pierpont 
,
Joan Steyermark,
David Nascene,
Matthew Bower,
Mary Ella Pierpont
,
Joan Steyermark,
David Nascene,
Matthew Bower,
Mary Ella Pierpont
This paper is made freely available by the publisher.
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