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References

1. Grange DK, Balfour IC, Chen SC, Wood EG. Familial syndrome of progressivearterial occlusive disease consistent with fibromuscular dysplasia, hypertension,congenital cardiac defects, bone fragility, brachysyndactyly, and learningdisabilities. Am J Med Genet. 1998 Feb 17;75(5):469-80.
2. Guo DC, Duan XY, Regalado ES, Mellor-Crummey L, Kwartler CS, Kim D, Lieberman K, de Vries BBA, Pfundt R, Schinzel A, Kotzot D, Shen X, Yang ML; University ofWashington Center for Mendelian Genomics, Bamshad MJ, Nickerson DA, Gornik HL,Ganesh SK, Braverman AC, Grange DK, Milewicz DM. Loss-of-Function Mutations inYY1AP1 Lead to Grange Syndrome and a Fibromuscular Dysplasia-Like VascularDisease. Am J Hum Genet. 2017 Jan 5;100(1):21-30. doi:10.1016/j.ajhg.2016.11.008.
3. Volonghi I, Frigerio M, Mardighian D, Gasparotti R, Del Zotto E, Giossi A,Costa P, Poli L, Jeannin G, Gregorini GA, Padovani A, Pezzini A. Grange syndrome:an identifiable cause of stroke in young adults. Am J Med Genet A. 2012Nov;158A(11):2894-8. doi: 10.1002/ajmg.a.35593.
4. Wallerstein R, Augustyn AM, Wallerstein D, Elton L, Tejeiro B, Johnson V,Lieberman K. A new case of Grange syndrome without cardiac findings. Am J MedGenet A. 2006 Jun 15;140(12):1316-20.
5. Weymann S, Yonekawa Y, Khan N, Martin E, Heppner FL, Schinzel A, Kotzot D.Severe arterial occlusive disorder and brachysyndactyly in a boy: a further case of Grange syndrome? Am J Med Genet. 2001 Mar 15;99(3):190-5.