Mutations in HYAL2, Encoding Hyaluronidase 2, Cause a Syndrome of Orofacial Clefting and Cor Triatriatum Sinister in Humans and Mice.
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| Title: | Mutations in HYAL2, Encoding Hyaluronidase 2, Cause a Syndrome of Orofacial Clefting and Cor Triatriatum Sinister in Humans and Mice. |
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| Authors: | Muggenthaler MM; RILD Wellcome Wolfson Centre, University of Exeter Medical School, Exeter, United Kingdom., Chowdhury B; Department of Biochemistry & Medical Genetics, University of Manitoba, Winnipeg, Manitoba, Canada., Hasan SN; Department of Biochemistry & Medical Genetics, University of Manitoba, Winnipeg, Manitoba, Canada., Cross HE; Department of Ophthalmology, University of Arizona College of Medicine, Tucson, Arizona, United States of America., Mark B; Department of Microbiology, University of Manitoba, Winnipeg, Manitoba, Canada., Harlalka GV; RILD Wellcome Wolfson Centre, University of Exeter Medical School, Exeter, United Kingdom., Patton MA; RILD Wellcome Wolfson Centre, University of Exeter Medical School, Exeter, United Kingdom.; Genetics Research Centre, St George's University London, London, United Kingdom., Ishida M; Genetics and Genomic Medicine, UCL Institute of Child Health, London, United Kingdom., Behr ER; Cardiovascular Sciences Research Centre, St George's University of London, London, United Kingdom., Sharma S; Cardiovascular Sciences Research Centre, St George's University of London, London, United Kingdom., Zahka K; Pediatric Cardiology, Cleveland Clinic, Cleveland, Ohio, United States of America., Faqeih E; Department of Pediatric Subspecialties, Children's Hospital, King Fahad Medical City, Riyadh, Saudi Arabia., Blakley B; Department of Otolaryngology, University of Manitoba, Winnipeg, Manitoba, Canada., Jackson M; Department of Small Animal and Materials Imaging Facility, University of Manitoba, Winnipeg, Manitoba, Canada., Lees M; Department of Clinical Genetics, Great Ormond Street Hospital, London, United Kingdom., Dolinsky V; Pharmacology & Therapeutics, University of Manitoba, Winnipeg, Manitoba, Canada.; Pediatrics & Child Health, University of Manitoba, Winnipeg, Manitoba, Canada., Cross L; Windows of Hope Genetic Information Centre, Holmes County, Ohio, United States of America., Stanier P; Genetics and Genomic Medicine, UCL Institute of Child Health, London, United Kingdom., Salter C; Human Genetics and Genomic Medicine, Faculty of Medicine, University of Southampton, Southampton, United Kingdom., Baple EL; RILD Wellcome Wolfson Centre, University of Exeter Medical School, Exeter, United Kingdom., Alkuraya FS; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.; Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia., Crosby AH; RILD Wellcome Wolfson Centre, University of Exeter Medical School, Exeter, United Kingdom., Triggs-Raine B; Department of Biochemistry & Medical Genetics, University of Manitoba, Winnipeg, Manitoba, Canada.; Pediatrics & Child Health, University of Manitoba, Winnipeg, Manitoba, Canada.; Manitoba Institute of Child Health, Winnipeg, Manitoba, Canada., Chioza BA; RILD Wellcome Wolfson Centre, University of Exeter Medical School, Exeter, United Kingdom. |
| Source: | PLoS genetics [PLoS Genet] 2017 Jan 12; Vol. 13 (1), pp. e1006470. Date of Electronic Publication: 2017 Jan 12 (Print Publication: 2017). |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Public Library of Science Country of Publication: United States NLM ID: 101239074 Publication Model: eCollection Cited Medium: Internet ISSN: 1553-7404 (Electronic) Linking ISSN: 15537390 NLM ISO Abbreviation: PLoS Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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