Mutations in MCT1 cDNA in patients with symptomatic deficiency in lactate transport

Muscle and Nerve

Volumn 23, Issue 1, 2000, Pages 90-97

  Merezhinskaya, Natalya ^a   Fishbein, William N ^a   Davis, John I ^a   Foellmer, John W ^a  

^a ARMED FORCES INSTITUTE OF PATHOLOGY   (United States)

Author keywords

Creatine kinase; Lactate transport; MCT1 mutations; Muscle cramping; Rhabdomyolysis

Indexed keywords

CARNITINE PALMITOYLTRANSFERASE; CREATINE KINASE; MESSENGER RNA;

ADULT; ARTICLE; CASE REPORT; COHORT ANALYSIS; ELECTROMYOGRAM; ERYTHROCYTE; EXERCISE; FATIGUE; GENE MUTATION; GENETIC DISORDER; HAND GRIP; HUMAN; LACTATE BLOOD LEVEL; MALE; MISSENSE MUTATION; MUSCLE CRAMP; MUSCLE INJURY; PHYSICAL EXAMINATION; PRIORITY JOURNAL; RACE DIFFERENCE; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SINGLE STRAND CONFORMATION POLYMORPHISM; THERMAL EXPOSURE; TRAINING;

ADULT; ARM; BIOLOGICAL TRANSPORT, ACTIVE; CARBOHYDRATE METABOLISM, INBORN ERRORS; CARRIER PROTEINS; DNA, COMPLEMENTARY; ELECTROPHORESIS, AGAR GEL; ERYTHROCYTES; HUMANS; LACTIC ACID; MALE; MIDDLE AGED; MONOCARBOXYLIC ACID TRANSPORTERS; MUSCLE, SKELETAL; MUTATION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; REGIONAL BLOOD FLOW; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RNA, MESSENGER;

EID: 0033970668     PISSN: 0148639X     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-4598(200001)23:1<90::AID-MUS12>3.0.CO;2-M     Document Type: Article

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