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Journal of the Neurological Sciences|April 30, 1998
Adult Sandhoff's disease: R505Q and I207V substitutions in the HEXB gene of the first Japanese caseA Hara, E Uyama, M Uchino, et al.
Radiation Research|March 1, 1992
The v-src oncogene may not be responsible for the increased radioresistance of hematopoietic progenitor cells expressing v-srcM A Santucci, P Anklesaria, S M Anderson, et al.
Neurology|February 5, 1999
GM2 gangliosidosis AB variant: clinical and biochemical studies of a Japanese patientH Sakuraba, K Itoh, M Shimmoto, et al.
Cell|April 3, 1992
Developmental defects in Gorlin syndrome related to a putative tumor suppressor gene on chromosome 9M R Gailani, S J Bale, D J Leffell, et al.
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