Search for other papers by Mabel E Bohórquez in
Google Scholar
PubMed
Search for other papers by Ana P Estrada in
Google Scholar
PubMed
Search for other papers by Jacob Stultz in
Google Scholar
PubMed
Search for other papers by Ruta Sahasrabudhe in
Google Scholar
PubMed
Search for other papers by John Williamson in
Google Scholar
PubMed
Search for other papers by Paul Lott in
Google Scholar
PubMed
Search for other papers by Carlos S Duque in
Google Scholar
PubMed
Search for other papers by Jorge Donado in
Google Scholar
PubMed
Search for other papers by Gilbert Mateus in
Google Scholar
PubMed
Search for other papers by Fernando Bolaños in
Google Scholar
PubMed
Search for other papers by Alejandro Vélez in
Google Scholar
PubMed
Search for other papers by Magdalena Echeverry in
Google Scholar
PubMed
Genome Center and Department of Biochemistry and Molecular Medicine, School of Medicine, University of California, Davis, California, USA
Fundación de Genética y Genómica, Medellín, Colombia
Search for other papers by Luis G Carvajal-Carmona in
Google Scholar
PubMed
( 4 ), there has not been conclusive evidence for the discovery of highly penetrant NMTC genes. Recently, two studies implicated a germline missense variant (G534E) in the HABP2 gene as the cause of familial NMTC ( 5 , 6 ). Gara and coworkers ( 5
Postgraduate Program in Health Sciences, Universidade Federal do Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil
Search for other papers by Luis Eduardo Barbalho de Mello in
Google Scholar
PubMed
Search for other papers by Thaise Nayane Ribeiro Carneiro in
Google Scholar
PubMed
Search for other papers by Aline Neves Araujo in
Google Scholar
PubMed
Search for other papers by Camila Xavier Alves in
Google Scholar
PubMed
Search for other papers by Pedro Alexandre Favoretto Galante in
Google Scholar
PubMed
Search for other papers by Vanessa Candiotti Buzatto in
Google Scholar
PubMed
Department of Clinical and Toxicological Analyses, Natal, Rio Grande do Norte, Brazil
Search for other papers by Maria das Graças de Almeida in
Google Scholar
PubMed
Search for other papers by Karina Marques Vermeulen-Serpa in
Google Scholar
PubMed
Department of Nutrition, Universidade Federal do Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil
Search for other papers by Sancha Helena de Lima Vale in
Google Scholar
PubMed
Search for other papers by Fernando José de Pinto Paiva in
Google Scholar
PubMed
Search for other papers by José Brandão-Neto in
Google Scholar
PubMed
Search for other papers by Janete Maria Cerutti in
Google Scholar
PubMed
reported FNMTC-associated chromosomal loci ( 3 , 15 , 16 , 17 , 18 ) and predisposing risk variants in over 100 genes, including SRGAP1 , CHEK2 , SRRM2 , TIFF-1/NKX2 , FOXE1 , NOP53 , HABP2 , ANO7 , CAV2 , KANK1 , PIK3CB , PKD1L1 , PTPRF
Search for other papers by Catherine Cardot Bauters in
Google Scholar
PubMed
Search for other papers by Emmanuelle Leteurtre in
Google Scholar
PubMed
Search for other papers by Bruno Carnaille in
Google Scholar
PubMed
Search for other papers by Christine Do Cao in
Google Scholar
PubMed
Search for other papers by Stéphanie Espiard in
Google Scholar
PubMed
Search for other papers by Malo Penven in
Google Scholar
PubMed
Search for other papers by Evelyne Destailleur in
Google Scholar
PubMed
Search for other papers by Isabelle Szuster in
Google Scholar
PubMed
Search for other papers by Tonio Lovecchio in
Google Scholar
PubMed
CHU Lille, Service de Biochimie Hormonologie, Métabolisme, Nutrition-Oncologie, Centre de Biologie Pathologie Génétique, Lille, France
Search for other papers by Julie Leclerc in
Google Scholar
PubMed
Search for other papers by Fredéric Frénois in
Google Scholar
PubMed
Search for other papers by Emmanuel Esquivel in
Google Scholar
PubMed
Search for other papers by Patricia L M Dahia in
Google Scholar
PubMed
Search for other papers by Emilie Ait-Yahya in
Google Scholar
PubMed
Search for other papers by Michel Crépin in
Google Scholar
PubMed
Search for other papers by Pascal Pigny in
Google Scholar
PubMed
et al . Multiple HABP2 variants in familial papillary thyroid carcinoma: contribution of a group of ‘thyroid checked’ controls . European Journal of Medical Genetics 2017 60 178 – 184 . ( https://doi.org/10.1016/j.ejmg.2017.01.001 ) 17