"
Diagnostic challenges in Salla disease"
written by Jessica N. Hartley, Michael S. Salman, Frances A. Booth, Lorne Seargeant, David A. Wenger, Jens Wrogemann, Aizeddin A. Mhanni,
published by
Open Journal of Genetics,
Vol.3 No.2C, 2013
has been cited by the following article(s):
[1]
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Prenatal hydrops fetalis associated with infantile free sialic acid storage disease due to a novel homozygous deletion in the SLC17A5 gene
Molecular Case Studies,
2021
DOI:10.1101/mcs.a006106
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