Publications

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Author Title [ Year(Asc)]
Filters: Author is Valivullah, Zaheer  [Clear All Filters]
2020
Al-Deri, N. et al. A novel homozygous variant in results in a neurodevelopmental disorder and disrupts TRAPP complex function. J Med Genet (2020). doi:10.1136/jmedgenet-2020-107016
2019
Kitzler, T. M. et al. COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humans. Hum Genet 138, 1105-1115 (2019).