Inheritance of low-frequency regulatory SNPs and a rare null mutation in exon-junction complex subunit RBM8A causes TAR
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Ana Cvejic | Panos Deloukas | Matthew E Hurles | Paul Bertone | Martijn H Breuning | Ni Huang | Chantal Thys | Kathleen Freson | Paquita Nurden | Myrto Kostadima | Dirk S Paul | Cornelis A Albers | P. Deloukas | M. Hurles | C. A. Albers | W. Ouwehand | J. Jolley | Paul Bertone | D. Stemple | P. Nurden | N. Debili | R. Favier | N. Huang | J. Sambrook | J. Stephens | A. Cvejic | R. Newbury-Ecob | C. Ruivenkamp | D. Paul | M. Breuning | P. Smethurst | C. Ghevaert | K. Freson | H. Schulze | C. Thys | I. Krapels | Willem H Ouwehand | Najet Debili | Ruth Newbury-Ecob | Cedric Ghevaert | Derek L Stemple | Harald Schulze | Gabriele Strauss | Claudia A L Ruivenkamp | G. Strauss | Jonathan C Stephens | Peter A Smethurst | Jennifer D Jolley | Rémi Favier | Janine Fiedler | Catherine M Hobbs | Graham Kiddle | Ingrid Krapels | Jennifer G Sambrook | Kenneth Smith | Christel van Geet | G. Kiddle | Myrto A. Kostadima | Catherine M. Hobbs | C. van Geet | Janine Fiedler | Kenneth Smith
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