Bitner-Glindzicz,Maria

Institution: UCL Institute of Child Health, UK

Top Collaborators: Steele-stallard HB, Luxon LM, Webster AR, Le Quesne Stabej P, Ambrose J, Coffey A, Emmerson J, Haralambous E, Hughes Y, Steel KP, Saihan Z, Rangesh N, Lenassi E, Claustres M, Roux AF, Landa P, Differ AM, Rajput K, Jenkins L

Research Interests: Genes, Syndrome, Hearing, Patients, Usher Syndrome, Disease, Gene, Mutation, Potassium, Hearing Loss, Inheritance, Retinitis, Retinitis Pigmentosa, Blindness, Diagnosis, Families, Mutations, Screening, Deafness, Eva