Gene symbol: MECP2. Disease: Rett syndrome (atypical).

Human genetics

Volumn 118, Issue 3-4, 2005, Pages 547-

  Penagarikano, O ^a   Martinez Bouzas, Cristina ^a   Mínguez, Mónica ^a   Sanz Parra, Arantza ^a   García Alegría, Eva ^a   Beristain, Elena ^a   Tejada, M Isabel ^a  

^a EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MECP2 PROTEIN, HUMAN; METHYL CPG BINDING PROTEIN 2;

ADOLESCENT; AMINO ACID SUBSTITUTION; ARTICLE; CASE REPORT; FEMALE; FRAGILE X SYNDROME; GENETICS; HOSPITALIZATION; HUMAN; LEARNING DISORDER; MENTAL DEFICIENCY; MISSENSE MUTATION; PHENOTYPE; RETT SYNDROME; STOP CODON;

ADOLESCENT; AMINO ACID SUBSTITUTION; CODON, NONSENSE; FEMALE; FRAGILE X SYNDROME; HUMANS; LEARNING DISORDERS; MENTAL RETARDATION; METHYL-CPG-BINDING PROTEIN 2; MUTATION, MISSENSE; PHENOTYPE; RETT SYNDROME; SEVERITY OF ILLNESS INDEX;

EID: 33644951525     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)