Charles E. Schwartz

Table 2. [SMS Pathogenic Variants Discussed in This GeneReview].

Jessica Albert, Charles E. Schwartz, Cornelius F. Boerkoel, 2013 .

Structural assessment of the effects of Amino Acid Substitutions on protein stability and protein-protein interaction

Emil Alexov, Anand K. Srivastava, Liangjiang Wang, 2010, Int. J. Comput. Biol. Drug Des..

High frequency of neurexin 1β signal peptide structural variants in patients with autism

Charles E. Schwartz, Edwin H. Cook, Jin Yan, 2006, Neuroscience Letters.

X-linked creatine transporter (SLC6A8) mutations in about 1% of males with mental retardation of unknown etiology

Charles E. Schwartz, Roger E. Stevenson, R. Stevenson, 2006, Human Genetics.

Genetics of X-Linked Intellectual Disability

Charles E. Schwartz, Luigi Boccuto, C. Schwartz, 2016 .

A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures

Yu Wang, Zhaoshi Jiang, Gregory M. Cooper, 2008, Nature Genetics.

Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans

Charles E. Schwartz, Eva Morava, Denise Horn, 2003, Nature Genetics.