Altered neurodevelopment associated with mutations of RSK2: A morphometric MRI study of Coffin-Lowry syndrome

Neurogenetics

Volumn 8, Issue 2, 2007, Pages 143-147

  Kesler, Shelli R ^a   Simensen, Richard J ^b   Voeller, Kytja ^b   Abidi, Fatima ^b   Stevenson, Roger E ^b   Schwartz, Charles E ^b   Reiss, Allan L ^a  

^a STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b GREENWOOD GENETIC CENTER   (United States)

Author keywords

Coffin Lowry syndrome; Hippocampus; MRI; RSK2; X linked mental retardation

Indexed keywords

PROTEIN; RIBOSOMAL S6 PROTEIN KINASE 2; UNCLASSIFIED DRUG;

ADULT; ARTICLE; BRAIN SIZE; CEREBELLUM; CHILD; CLINICAL ARTICLE; COFFIN LOWRY SYNDROME; CONTROLLED STUDY; FEMALE; GENE MUTATION; HIPPOCAMPUS; HUMAN; MALE; MORPHOMETRICS; NERVE CELL DIFFERENTIATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL;

ADULT; BRAIN; CEREBELLUM; CHILD; COFFIN-LOWRY SYNDROME; CONSERVED SEQUENCE; FEMALE; HETEROZYGOTE DETECTION; HIPPOCAMPUS; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; MUTATION; SMALL-CONDUCTANCE CALCIUM-ACTIVATED POTASSIUM CHANNELS;

EID: 33847661648     PISSN: 13646745     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10048-007-0080-6     Document Type: Article

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