HIGHLIGHTS
- who: Adil U Rehman and collaborators from the Department of Biotechnology and Genetic Engineering, University of Science and Technology (KUST), Center for Genetics and Inherited Diseases, Taibah University, Al-Madinah Al-Munwarah, Saudi Arabia have published the research work: The Expansion of the Spectrum in Stuttering Disorders to a Novel ARMC Gene Family (ARMC3), in the Journal: Genes 2022, 13, 2299. of 13/05/2022
- what: The authors report as novel candidate gene causing the stuttering phenotype. may lead to neurodevelopmental disorders including stuttering in humans. The authors provide clinical and molecular findings of a . . .
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