Lowe syndrome: Case report of a patient with a novel mutation in the OCRL gene
By: Grace Angeline Malarnangai Kularatnam, Vindya Subasinghe, Dilanthi Hewa Warawitage, Kandana Liyanage Subhashinie Jayasena, Florian Recker, Eresha Anandanie Jasinge, Samantha Waidyanatha and Michael Ludwig
Open Access
|Sep 2017Authors
Grace Angeline Malarnangai Kularatnam
District General Hospital Matara, Sri Lanka
Kandana Liyanage Subhashinie Jayasena
Lady Ridgeway Hospital Colombo, Sri Lanka
DOI: https://doi.org/10.4038/sljch.v46i3.8334 | Journal eISSN: 2386-110X
Language: English
Page range: 281 - 283
Published on: Sep 5, 2017
Published by: Sri Lanka College of Paediatricians
In partnership with: Paradigm Publishing Services
© 2017 Grace Angeline Malarnangai Kularatnam, Vindya Subasinghe, Dilanthi Hewa Warawitage, Kandana Liyanage Subhashinie Jayasena, Florian Recker, Eresha Anandanie Jasinge, Samantha Waidyanatha, Michael Ludwig, published by Sri Lanka College of Paediatricians
This work is licensed under the Creative Commons License.