Associated Papers
Non-polyalanine repeat mutation in PHOX2B is detected in autopsy cases of sudden unexpected infant death.
Ueda A et al.
Plos One, 2022
35486589 (PubMed )
Supplement: pone.0267751.s001.xls › SIDS3-full
Identification of a Pathogenic TGFBR2 Variant in a Patient With Loeys-Dietz Syndrome.
Luo X et al.
Frontiers in Genetics, 2020
32528524 (PubMed )
Supplement: Data_Sheet_1.XLSX › variants_in_candidate_genes
Novel polymorphisms in the myosin light chain kinase gene confer risk for acute lung injury.
Gao L et al.
American Journal of Respiratory Cell and Molecular Biology, 2006
16399953 (PubMed )
Supplement: gao_2005-0404oc_online_suppl.pdf
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