Contribution of SHANK3 mutations to autism spectrum disorder.

Moessner R, Marshall CR, Sutcliffe JS, Skaug J, Pinto D, Vincent J, Zwaigenbaum L, Fernandez B, Roberts W, Szatmari P, Scherer SW
Am J Hum Genet. 2007 81 (6): 1289-97

PMID: 17999366 · PMCID: PMC2276348 · DOI:10.1086/522590

MeSH Terms (16)

Autistic Disorder Carrier Proteins Chromosome Mapping Chromosomes, Human, Pair 14 Chromosomes, Human, Pair 20 Chromosomes, Human, Pair 22 DNA Female Genetic Variation Humans Male Mutation Nerve Tissue Proteins Pedigree Sequence Deletion Translocation, Genetic

Connections (1)

This publication is referenced by other Labnodes entities:

Links