Associated Papers
A Novel Missense Mutation in TNNI3K Causes Recessively Inherited Cardiac Conduction Disease in a Consanguineous Pakistani Family.
Ramzan S et al.
Genes, 2021
The paradox of cancer genes in non-malignant conditions: implications for precision medicine.
Adashek JJ et al.
Genome Medicine, 2020
Growth factor and receptor malfunctions associated with human genetic deafness.
Naz S et al.
Clinical Genetics, 2020
Genetic screening as an adjunct to universal newborn hearing screening: literature review and implications for non-congenital pre-lingual hearing loss.
D'Aguillo C et al.
International Journal of Audiology, 2019
Genetic causes of moderate to severe hearing loss point to modifiers.
Naz S et al.
Clinical Genetics, 2017
A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss.
Mujtaba G et al.
Journal of Medical Genetics, 2015
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