Fingerprint
Dive into the research topics of 'NTNG1 mutations are a rare cause of Rett Syndrome'. Together they form a unique fingerprint.- Sort by
- Weight
- Alphabetically
NTNG1 mutations are a rare cause of Rett Syndrome
H.L. Archer, J.C. Evans, D.S. Millar, P.W. Thompson, A.M. Kerr, Helen Leonard, J. Christodoulou, David Ravine, L. Lazarou, L. Grove, C. Verity, S.D. Whatley, D.T. Pilz, J.R. Sampson, A.J. Clarke
Research output: Contribution to journal › Article › peer-review
39
Citations
(Scopus)