Seven functional classes of barth syndrome mutation

Human Molecular Genetics

Volumn 22, Issue 3, 2013, Pages 483-492

  Whited, Kevin ^a   Baile, Matthew G ^a   Currier, Pamela ^a   Claypool, Steven M ^a  

^a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN; TAFAZZIN PROTEIN; UNCLASSIFIED DRUG;

ALLELE; ARTICLE; BARTH SYNDROME; CHEMICAL ANALYSIS; CONTROLLED STUDY; CYTOLOGY; MITOCHONDRION; NONHUMAN; PRIORITY JOURNAL; PROTEIN LOCALIZATION; TEMPERATURE;

ACYLTRANSFERASES; ALLELES; BARTH SYNDROME; CARDIOLIPINS; CARDIOMYOPATHIES; HUMANS; KINETICS; LYSOPHOSPHOLIPIDS; MITOCHONDRIA; MUTATION, MISSENSE; NEUTROPENIA; PROTEIN CONFORMATION; SACCHAROMYCES CEREVISIAE; SACCHAROMYCES CEREVISIAE PROTEINS; TEMPERATURE; TRANSCRIPTION FACTORS;

SACCHAROMYCES CEREVISIAE;

EID: 84872372503     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/dds447     Document Type: Article

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