MECP2 mutations in Malaysian Rett syndrome patients
Through the use of post-PCR high-performance liquid chromatography, 65 percent of 20 RS patients were found to have mutation(s) in the MECP2.
Saved in:
Main Authors: | Fong, C.B., Thong, M.K., Sam, C.K., Mohamed Noor, M.N., Ariffin, R. |
---|---|
Format: | Article |
Published: |
Stamford Publishing Pte Ltd / Singapore Medical Association
2009
|
Subjects: | |
Online Access: | http://eprints.um.edu.my/1119/ http://www.ncbi.nlm.nih.gov/pubmed/19495527 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Structural and biophysical characterisations of MeCP2 MBD mutants that correlate with Rett syndrome
by: Chia, Jyh Yea
Published: (2016) -
Epidermal growth factor receptor mutations in lung adenocarcinoma in Malaysian patients
by: Liam, C.K., et al.
Published: (2013) -
Adenylosuccinate lyase deficiency in a Malaysian patient, with novel adenylosuccinate lyase gene mutations
by: Chen, B.C., et al.
Published: (2010) -
Co-inheritance of variants/mutations in Malaysian patients with Crohn s disease
by: Chua, K.H., et al.
Published: (2012) -
Genetic mutations in dysferlinopathy in a Malaysian population
by: Looi, R.Y., et al.
Published: (2010)