Mitochondrial and ion channel gene alterations in autism

Biochimica et Biophysica Acta - Bioenergetics

Volumn 1817, Issue 10, 2012, Pages 1796-1802

  Smith, Moyra ^a   Flodman, Pamela L ^a   Gargus, John J ^a   Simon, Mariella T ^a   Verrell, Kimberley ^a   Haas, Richard ^b   Reiner, Gail E ^b   Naviaux, Robert ^b   Osann, Katherine ^a   Spence, M Anne ^a   Wallace, Douglas C ^c  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

Autism; Calcium channel; Copy number variants (CNVs); Mitochondria; OXPHOS; Synapses

Indexed keywords

ION CHANNEL;

AUTISM; BIOENERGY; CALCIUM TRANSPORT; CHROMOSOME ANALYSIS; CHROMOSOME REARRANGEMENT; CONFERENCE PAPER; CONTROLLED STUDY; COPY NUMBER VARIATION; FLUORESCENCE IN SITU HYBRIDIZATION; GENE FREQUENCY; GENE MUTATION; HUMAN; ION TRANSPORT; MAJOR CLINICAL STUDY; METABOLISM; MICROARRAY ANALYSIS; MITOCHONDRION; OXIDATIVE PHOSPHORYLATION; PRIORITY JOURNAL; SYNAPSE; SYNAPTIC POTENTIAL;

AUTISTIC DISORDER; CHILD; CHILD, PRESCHOOL; FEMALE; GENE DOSAGE; GENOME-WIDE ASSOCIATION STUDY; HUMANS; ION CHANNELS; ION TRANSPORT; MALE; MITOCHONDRIAL PROTEINS; OXIDATIVE PHOSPHORYLATION; SYNAPSES;

EID: 84864704318     PISSN: 00052728     EISSN: 18792650     Source Type: Journal    
DOI: 10.1016/j.bbabio.2012.04.004     Document Type: Conference Paper

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