N Wakamatsu

Late infantile Hirschsprung disease–mental retardation syndrome with a 3-bp deletion in ZFHX1B

N. Wakamatsu, M Nagaya, M. Kishikawa, 2002, Neurology.

Dramatically different phenotypes in mouse models of human Tay-Sachs and Sandhoff diseases.

N Hanai, J. Marth, A. Peterson, 1996, Human molecular genetics.