P.B. Munroe
Department of Pediatrics
University College London Medical School
The Rayne Institute
United Kingdom
Name/email consistency: high
- Mutations in the gene encoding the human matrix Gla protein cause Keutel syndrome. Munroe, P.B., Olgunturk, R.O., Fryns, J.P., Van Maldergem, L., Ziereisen, F., Yuksel, B., Gardiner, R.M., Chung, E. Nat. Genet. (1999)
- Spectrum of mutations in the Batten disease gene, CLN3. Munroe, P.B., Mitchison, H.M., O'Rawe, A.M., Anderson, J.W., Boustany, R.M., Lerner, T.J., Taschner, P.E., de Vos, N., Breuning, M.H., Gardiner, R.M., Mole, S.E. Am. J. Hum. Genet. (1997)