Cargando…
Duplication of the NPHP1 gene in patients with autism spectrum disorder and normal intellectual ability: a case series
Autism spectrum disorder is a neurodevelopmental disorder characterized by impairments in social interactions, reduced verbal communication abilities, stereotyped repetitive behaviors, and restricted interests. It is a complex condition caused by genetic and environmental factors; the high heritabil...
Autores principales: | Yasuda, Yuka, Hashimoto, Ryota, Fukai, Ryoko, Okamoto, Nobuhiko, Hiraki, Yoko, Yamamori, Hidenaga, Fujimoto, Michiko, Ohi, Kazutaka, Taniike, Masako, Mohri, Ikuko, Nakashima, Mitsuko, Tsurusaki, Yoshinori, Saitsu, Hirotomo, Matsumoto, Naomichi, Miyake, Noriko, Takeda, Masatoshi |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131154/ https://www.ncbi.nlm.nih.gov/pubmed/25126106 http://dx.doi.org/10.1186/s12991-014-0022-2 |
Ejemplares similares
-
Gene expression analysis in lymphoblasts derived from patients with autism spectrum disorder
por: Yasuda, Yuka, et al.
Publicado: (2011) -
Performance Comparison of Bench-Top Next Generation Sequencers Using Microdroplet PCR-Based Enrichment for Targeted Sequencing in Patients with Autism Spectrum Disorder
por: Koshimizu, Eriko, et al.
Publicado: (2013) -
Two novel homozygous RAB3GAP1 mutations cause Warburg micro syndrome
por: Imagawa, Eri, et al.
Publicado: (2015) -
A Brief Assessment of Intelligence Decline in Schizophrenia As Represented by the Difference between Current and Premorbid Intellectual Quotient
por: Ohi, Kazutaka, et al.
Publicado: (2017) -
ANKRD11 variants cause variable clinical features associated with KBG syndrome and Coffin–Siris-like syndrome
por: Miyatake, Satoko, et al.
Publicado: (2017)