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Analysis of a patient with X-linked mental retardation by next generation sequencing / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 257-260, 2018.
Article in Chinese | WPRIM | ID: wpr-687965
ABSTRACT
<p><b>OBJECTIVE</b>To explore the clinical and genetic features of a Chinese boy featuring X-linked mental retardation.</p><p><b>METHODS</b>Clinical features of the patient were analyzed. The DNA of the patient and his parents was extracted and sequenced by next generation sequencing. The results were validated and analyzed with software.</p><p><b>RESULTS</b>The child displayed X-linked mental retardation. Sequencing showed the patient has carried a c.455T>C (p.L152P) mutation of the GRIA3 gene inherited from his mother.</p><p><b>CONCLUSION</b>The c.455T>C (p.L152P) mutation of the GRIA3 gene probably underlies the X-linked mental retardation in this child.</p>
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Receptors, AMPA / Mental Retardation, X-Linked / High-Throughput Nucleotide Sequencing / Genetics / Methods / Mutation Limits: Child, preschool / Humans / Male Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2018 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Receptors, AMPA / Mental Retardation, X-Linked / High-Throughput Nucleotide Sequencing / Genetics / Methods / Mutation Limits: Child, preschool / Humans / Male Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2018 Type: Article