Open AccessDifferent Clinical Faces of the Same Gene Mutation: Fragile X Mental Retardation 1 Disorders
Author(s) -
Burcu Asma,
Berk Özyılmaz,
Feray Güleç Uyaroğlu
Publication year - 2021
Publication title -
turkish journal of neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.144
H-Index - 4
eISSN - 1309-2545
pISSN - 1301-062X
DOI - 10.4274/tnd.2021.58234
Subject(s) - fragile x syndrome , fragile x , genetics , ataxia , medicine , autism , chromosomal fragile site , fmr1 , allele , x chromosome , trinucleotide repeat expansion , disease , asymptomatic , mutation , gene , psychiatry , chromosome , biology
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