Authors: Indo, Y Mardy, S Miura, Y Moosa, A Ismail, EAR Toscano, E Andria, G Pavone, V Brown, DL Brooks, A Endo, F Matsuda, I

Citation: Y. Indo et al., Congenital insensitivity to pain with anhidrosis (CIPA): Novel mutations of the TRK4 (NTRK1) gene, a putative uniparental disomy, and a linkage of the mutant TRKA and PKLR genes in a family with CIPA and pyruvate kinase deficiency, HUM MUTAT, 18(4), 2001, pp. 308-318

Authors: Haider, MZ Moosa, A Dalal, H Habib, Y Reynold, L

Citation: Mz. Haider et al., Gene deletion patterns in spinal muscular atrophy patients with different clinical phenotypes, J BIOMED SC, 8(2), 2001, pp. 191-196

Authors: Mardy, S Miura, Y Endo, F Matsuda, I Sztriha, L Frossard, P Moosa, A Ismail, EAR Macaya, A Andria, G Toscano, E Gibson, W Graham, GE Indo, Y

Citation: S. Mardy et al., Congenital insensitivity to pain with anhidrosis: Novel mutations in the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor, AM J HU GEN, 64(6), 1999, pp. 1570-1579

Authors: Ismail, EAR Al-Shammari, N Amin, JT Moosa, A

Citation: Ear. Ismail et al., Congenital insensitivity to pain with anhidrosis: Lack of eccrine sweat gland innervation confirmed (vol 13, pg 243, 1998), J CHILD NEU, 13(12), 1998, pp. 632-632