Browsing Journal Articles by Author "Tee, LJ"

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    • The Transmembrane Protein Meckelin (MKS3) Is Mutated In Meckel-Gruber Syndrome And The Wpk Rat. 

      Johnson, CA; Harris, PC; Gattone VH, 2nd; Maher, ER; Kelly, DA; Attie-Bitach, T; Torres, VE; Trembath, RC; Algazali, L; Cox, P; Miller, CA; Bucourt, M; McKeown, C; Woods, CG; Bennett, CP; Batman, PA; Malik, Sharif S; Punyashthiti, R; Pasha, S; Ward, CJ; Aligianis, IA; Lilliquist, S; Gissen, P; Goranson, E; Morgan, NV; Whelan, S; Maina, EN; McKee, BM; Tee, LJ; Consugar, M; Smith, UM (Department of Biochemistry, 2006)
      Meckel-Gruber syndrome is a severe autosomal, recessively inherited disorder characterized by bilateral renal cystic dysplasia, developmental defects of the central nervous system (most commonly occipital encephalocele), ...