论文信息 - De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder - 字舞流文

De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder

Rachel L. Taylor | R. Pfundt | M. Reijnders | B. D. de Vries | M. Bitner-Glindzicz | T. Strom | D. Baralle | J. Clayton-Smith | H. Brunner | C. Nellåker | D. Wieczorek | L. Bird | S. Twigg | A. Wilkie | S. Küry | P. J. van der Spek | S. McGowan | A. de Burca | C. Ruivenkamp | B. Kerr | S. Douzgou | M. Lees | E. Blair | J. Goos | I. Mathijssen | K. Cremer | H. Engels | B. Isidor | G. Santen | S. Kant | K. Helbig | M. Sinnema | M. Alders | C. Marcelis | K. Chandler | N. Cooper | C. Deshpande | J. Eason | A. Henderson | S. Joss | A. Kraus | S. McLean | K. Miller | S. Wall | A. Stegmann | K. Payne | M. V. van Dooren | P. Terhal | M. Koopmans | S. Mercimek-Andrews | E. Calpena | P. Edery | C. Schluth-Bolard | K. Tatton-Brown | H. Lüdecke | Kimberly Nugent | B. Mikat | P. Lakeman | M. Steinraths | K. Radtke | S. Swagemakers | M. Kozenko | R.O. Littlejohn | Nils Koelling | M. Harline | M. Klaassens | Lauren Brick | Patrick Yap | M. Alvi | Kelly Radtke | H. Lüdecke | Phillis Lakeman | R. Taylor | K. Miller | Scott McLean | Margot R. F. Reijnders | S. Mercimek‐Andrews