The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat
Ursula M. Smith(University of Birmingham), Mark Consugar(Mayo Clinic), Louise Tee(University of Birmingham), Brandy M McKee(Indiana University School of Medicine), Esther N. Maina(University of Birmingham), Shelly Whelan(Mayo Clinic), Neil V. Morgan(University of Birmingham), Erin Goranson(Mayo Clinic), Paul Gissen(Birmingham Children's Hospital), Stacie Lilliquist(Mayo Clinic), Irene A. Aligianis(University of Birmingham), Christopher J. Ward(Mayo Clinic), Shanaz Pasha(University of Birmingham), Rachaneekorn Punyashthiti(Mayo Clinic), Saghira Malik Sharif(St James's University Hospital), P A Batman(Bradford Royal Infirmary), Christopher Bennett(St James's University Hospital), C. Geoffrey Woods(Addenbrooke's Hospital), C McKeown(Birmingham Women's Hospital), Martine Bucourt(Hôpital Jean-Verdier), Caroline A. Miller(Indiana University School of Medicine), P. Cox(Birmingham Women's Hospital), Lihadh Al‐Gazali(United Arab Emirates University), Richard C. Trembath(University of Leicester), Vicente E. Torres(Mayo Clinic), Tania Attié‐Bitach(Hôpital Necker-Enfants Malades), Déirdre Kelly(Birmingham Children's Hospital), Eamonn R. Maher(University of Birmingham), Vincent H. Gattone(Indiana University School of Medicine), Peter C. Harris(Mayo Clinic), Colin A. Johnson(University of Birmingham)
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