Open AccessESOPHAGEAL MOTILITY DISTURBANCES IN CHILDREN WITH RETT SYNDROME: CORRELATION WITH X‐LINKED METHYL CPG BINDING PROTEIN (MECP2) GENE MUTATIONS
Author(s) -
Fortunato John E,
Darbari Anil,
Desbiens John,
Bibat Geni,
Naidu Sakkubai,
Cuffari Carmen
Publication year - 2005
Publication title -
journal of pediatric gastroenterology and nutrition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.206
H-Index - 131
eISSN - 1536-4801
pISSN - 0277-2116
DOI - 10.1097/01.mpg.0000181946.55344.ff
Subject(s) - rett syndrome , mecp2 , failure to thrive , dysphagia , medicine , gastroenterology , pathology , gene , phenotype , surgery , genetics , biology