Kularatnam, G.A.M., Subasinghe, V., Warawitage, D.H., Jayasena, K.L.S., Recker, F., Jasinge, E.A., Waidyanatha, S. and Ludwig, M., 2017. Lowe syndrome: Case report of a patient with a novel mutation in the OCRL gene. Sri Lanka Journal of Child Health, 46(3), pp.281–283. DOI: http://doi.org/10.4038/sljch.v46i3.8334

Kularatnam GAM, Subasinghe V, Warawitage DH, Jayasena KLS, Recker F, Jasinge EA, et al.. Lowe syndrome: Case report of a patient with a novel mutation in the OCRL gene. Sri Lanka Journal of Child Health. 2017;46(3):281–3. DOI: http://doi.org/10.4038/sljch.v46i3.8334

Kularatnam, G. A. M., Subasinghe, V., Warawitage, D. H., Jayasena, K. L. S., Recker, F., Jasinge, E. A., … Ludwig, M. (2017). Lowe syndrome: Case report of a patient with a novel mutation in the OCRL gene. Sri Lanka Journal of Child Health, 46(3), 281–283. DOI: http://doi.org/10.4038/sljch.v46i3.8334

1. Kularatnam GAM, Subasinghe V, Warawitage DH, et al.. Lowe syndrome: Case report of a patient with a novel mutation in the OCRL gene. Sri Lanka Journal of Child Health. 2017;46(3):281-283. DOI: http://doi.org/10.4038/sljch.v46i3.8334

Kularatnam GAM and others, ‘Lowe Syndrome: Case Report of a Patient with a Novel Mutation in the OCRL Gene’ (2017) 46 Sri Lanka Journal of Child Health 281 DOI: http://doi.org/10.4038/sljch.v46i3.8334

Kularatnam, Grace Angeline Malarnangai, Vindya Subasinghe, Dilanthi Hewa Warawitage, Kandana Liyanage Subhashinie Jayasena, Florian Recker, Eresha Anandanie Jasinge, Samantha Waidyanatha, and Michael Ludwig. 2017. “Lowe Syndrome: Case Report of a Patient with a Novel Mutation in the OCRL Gene”. Sri Lanka Journal of Child Health 46 (3): 281–83. DOI: http://doi.org/10.4038/sljch.v46i3.8334

Kularatnam, Grace Angeline Malarnangai, Vindya Subasinghe, Dilanthi Hewa Warawitage, Kandana Liyanage Subhashinie Jayasena, Florian Recker, Eresha Anandanie Jasinge, Samantha Waidyanatha, and Michael Ludwig. “Lowe Syndrome: Case Report of a Patient with a Novel Mutation in the OCRL Gene”. Sri Lanka Journal of Child Health 46, no. 3 (2017): 281–83. DOI: http://doi.org/10.4038/sljch.v46i3.8334

Kularatnam, G A M, et al.. “Lowe syndrome: Case report of a patient with a novel mutation in the OCRL gene”. Sri Lanka Journal of Child Health, vol. 46, no. 3, 2017, pp. 281–83. DOI: http://doi.org/10.4038/sljch.v46i3.8334