2 results for author:"Gollob T." in Literature citations
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| Novel PRKAG2 mutation responsible for the genetic syndrome of ventricular preexcitation and conduction system disease with childhood onset and absence of cardiac hypertrophy. Gollob M.H., Seger J.J., Gollob T.N., Tapscott T., Gonzales O., Bachinski L., Roberts R. Circulation 104:3030-3033(2001) · UniProtKB (1) · Mapped (5) |
| Identification of a gene responsible for familial Wolff-Parkinson-White syndrome. Gollob M.H., Green M.S., Tang A.S.-L., Gollob T., Karibe A., Al Sayegh A.H., Ahmad F., Lozado R., Shah G., Fananapazir L. et al. N. Engl. J. Med. 344:1823-1831(2001) · UniProtKB (1) |