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Novel human pathological mutations. Gene symbol: MECP2. Disease: Rett Syndrome.

Authors :
Khajuria R
Sapra S
Ghosh M
Gupta N
Gulati S
Kalra V
Kabra M
Source :
Human genetics [Hum Genet] 2010 Jan; Vol. 127 (1), pp. 117.
Publication Year :
2010

Subjects

Subjects :
Base Sequence
Codon genetics
Frameshift Mutation
Humans
India
Molecular Sequence Data
Sequence Analysis, DNA
Methyl-CpG-Binding Protein 2 genetics
Mutagenesis, Insertional
Rett Syndrome genetics

Details

Language :
English
ISSN :
1432-1203
Volume :
127
Issue :
1
Database :
MEDLINE
Journal :
Human genetics
Publication Type :
Academic Journal
Accession number :
20108429

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