Mutations in FLVCR2 Are Associated with Proliferative Vasculopathy and Hydranencephaly-Hydrocephaly Syndrome (Fowler Syndrome) - Concepedia

Concepedia

Publication | Open Access

Mutations in FLVCR2 Are Associated with Proliferative Vasculopathy and Hydranencephaly-Hydrocephaly Syndrome (Fowler Syndrome)

DOI Full Paper Access

81

Citations

23

References

2010

Year

Esther Meyer, Christopher J. Ricketts, Neil V. Morgan, Mark R. Morris, Shanaz Pasha, Louise Tee, Fatimah Rahman, Anne Bazin, Bettina Bessières, Pierre Déchelotte,

The American Journal of Human Genetics

Flvcr2 Are AssociatedHydranencephaly-hydrocephaly SyndromeFowler SyndromeGenetic DisorderGeneticsPathogenesisInherited Metabolic DiseasePathologyVascular BiologyDisease Gene IdentificationMedicineClinical Genetics

References

	Year	Citations

Page 1

Page 1