Funder
Maryland Stem Cell Research Fund (MSCRF)
RO1
Publisher
Public Library of Science (PLoS)
Reference50 articles.
1. Hypomorphic promoter mutation in PIGM causes inherited glycosylphosphatidylinositol deficiency;AM Almeida;NatMed,2006
2. Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome;PM Krawitz;NatGenet,2010
3. Mutations in PIGO, a member of the GPI-anchor-synthesis pathway, cause hyperphosphatasia with mental retardation;PM Krawitz;American journal of human genetics,2012
4. The phenotype of a germline mutation in PIGA: the gene somatically mutated in paroxysmal nocturnal hemoglobinuria;JJ Johnston;American journal of human genetics,2012
5. Early Frameshift Mutation in PIGA Identified in a Large XLID Family Without Neonatal Lethality;S Belet;Human mutation,2014
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