Mutations in the KDM5C ARID Domain and Their Plausible Association with Syndromic Claes-Jensen-Type Disease.

Mutations in the KDM5C ARID Domain and Their Plausible Association with Syndromic Claes-Jensen-Type Disease. Int J Mol Sci. 2015 Nov 13; 16(11):27270-87.

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subject areas

Amino Acid Sequence
Conserved Sequence
Evolution, Molecular
Genetic Association Studies
Histone Demethylases
Humans
Mental Retardation, X-Linked
Models, Molecular
Molecular Sequence Data
Mutation
Mutation, Missense
Protein Binding
Protein Conformation
Protein Denaturation
Protein Folding
Protein Interaction Domains and Motifs
Sequence Alignment
Structure-Activity Relationship

authors with profiles

Emil Georgiev Alexov
Tugba Gul Kucukkal