Mustafa Sahin, Ph.D., M.D.
This page shows the publications Mustafa Sahin has written about Genotype.
Chronic mTORC1 inhibition rescues behavioral and biochemical deficits resulting from neuronal Depdc5 loss in mice. Hum Mol Genet. 2019 09 01; 28(17):2952-2964.
Genetic Etiologies, Diagnosis, and Treatment of Tuberous Sclerosis Complex. Annu Rev Genomics Hum Genet. 2019 08 31; 20:217-240.
Low-level mosaicism in tuberous sclerosis complex: prevalence, clinical features, and risk of disease transmission. Genet Med. 2019 11; 21(11):2639-2643.
Tuberous Sclerosis Complex Genotypes and Developmental Phenotype. Pediatr Neurol. 2019 07; 96:58-63.
Clinical and genetic characterization of AP4B1-associated SPG47. . 2018 02; 176(2):311-318.
Tuberous sclerosis complex. Pediatr Clin North Am. 2015 Jun; 62(3):633-48.
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