Scrutinizing the molecular, biochemical, and cytogenetic attributes in subjects with Rett syndrome (RTT) and their mothers

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Published inEpilepsy & Behavior Vol. 111; p. 107277
Main Authors Karthick Kumar Alagamuthu, Vijaya Anand Arumugam, Balamuralikrishnan Balasubramanian, Sankar Kathannan, Sasikala Keshavarao, Murugesh Easwaran, Sureshkumar Shanmugam, Haripriya Kuchi Bhotla, Shafiahammedkhan Mustaqahamed, Arun Meyyazhagan, Manikantan Pappusamy, Tanushri Kaul
Format Journal Article
LanguageJapanese
Published Elsevier BV 01.10.2020
Subjects
Online AccessGet full text
ISSN1525-5050
DOI10.1016/j.yebeh.2020.107277

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Author Sureshkumar Shanmugam
Haripriya Kuchi Bhotla
Manikantan Pappusamy
Balamuralikrishnan Balasubramanian
Sankar Kathannan
Murugesh Easwaran
Tanushri Kaul
Vijaya Anand Arumugam
Shafiahammedkhan Mustaqahamed
Sasikala Keshavarao
Karthick Kumar Alagamuthu
Arun Meyyazhagan
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StartPage 107277
SubjectTerms Adolescent
Child
Child, Preschool
Cytogenetic Analysis
Female
Humans
In Situ Hybridization, Fluorescence
Methyl-CpG-Binding Protein 2
Molecular Diagnostic Techniques
Mothers
Mutation
Rett Syndrome
Young Adult
Title Scrutinizing the molecular, biochemical, and cytogenetic attributes in subjects with Rett syndrome (RTT) and their mothers
URI https://cir.nii.ac.jp/crid/1870302167848598272
Volume 111
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