Histological and molecular characterisation of hypotonia in adult Ts1Cje mouse model for down syndrome

Down syndrome (DS) is a genetic disorder caused by presence of extra copy of human chromosome 21 (Hsa21), a condition termed as trisomy 21. It is characterised by several number of clinical phenotypes such as intellectual disability, characteristic sets of facial features, cardiac defects and differ...

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Bibliographic Details
Main Author: Bala, Usman
Format: Thesis
Published: 2016
Online Access:http://psasir.upm.edu.my/id/eprint/66388/1/FPSK%202016%201%20IR.pdf
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