Ontology highlight
ABSTRACT:
SUBMITTER: Milic Rasic V
PROVIDER: S-EPMC4413439 | biostudies-literature | 2014 Dec
REPOSITORIES: biostudies-literature
Milic Rasic V V Vojinovic D D Pesovic J J Mijalkovic G G Lukic V V Mladenovic J J Kosac A A Novakovic I I Maksimovic N N Romac S S Todorovic S S Savic Pavicevic D D
Balkan journal of medical genetics : BJMG 20141201 2
Duchenne muscular dystrophy (DMD) is the most common form of muscular dystrophy during childhood. Mutations in dystrophin (DMD) gene are also recognized as a cause of cognitive impairment. We aimed to determine the association between intelligence level and mutation location in DMD genes in Serbian patients with DMD. Forty-one male patients with DMD, aged 3 to 16 years, were recruited at the Clinic for Neurology and Psychiatry for Children and Youth in Belgrade, Serbia. All patients had defined ...[more]