Mutations in FLVCR2 Are Associated with Proliferative Vasculopathy and Hydranencephaly-Hydrocephaly Syndrome (Fowler Syndrome)
Esther Meyer(University of Copenhagen), Eamonn R. Maher(Aston University), Pierre Déchelotte(Inserm), Fatimah Rahman, Mark R. Morris(University of Wolverhampton), Richard C. Trembath(King's College London), Louise Tee(University of Birmingham), Anne Bazin(Centre Hospitalier Sainte-Anne), P. Cox(Birmingham Women's Hospital), Tamás Marton(Birmingham Women's Hospital), Denise Williams(Birmingham Women's Hospital), Catherine Fallet‐Bianco(National Institute of Child Health), Christopher J. Ricketts(National Cancer Institute), Shanaz Pasha(University of Birmingham), Bettina Bessières, Mudher Al‐Adnani(Sheffield Children's NHS Foundation Trust), Neil V. Morgan(University of Birmingham), Mohamed Taher Yacoubi(Hôpital Farhat Hached), David Tannahill(Wellcome Sanger Institute)
Cited by 83
Related Papers
Nanopore sequencing and assembly of a human genome with ultra-long reads
|Nature Biotechnology|2018|2.1k
Prevalence of eating disorders over the 2000–2018 period: a systematic literature review
|American Journal of Clinical Nutrition|2018|1.7k
A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1
|Nature Genetics|2010|1.1k
The Somatic Genomic Landscape of Chromophobe Renal Cell Carcinoma
|Cancer Cell|2014|867