The natural history of homocystinura due to cystathionine β-synthase deficiency

American Journal of Human Genetics

Volumn 37, Issue 1, 1985, Pages 1-31

  Mudd, S H ^a   Skovby, F ^a   Levy, H L ^a  

^a NATIONAL INSTITUTE OF MENTAL HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYSTATHIONINE BETA SYNTHASE; PYRIDOXINE; DIAGNOSTIC AGENT; METHIONINE;

CONGENITAL DISORDER; CYSTATHIONINE SYNTHETASE; ENZYME DEFICIENCY; ETIOLOGY; HEREDITY; HOMOCYSTINURIA; HUMAN; MAJOR CLINICAL STUDY; NEWBORN SCREENING; PRIORITY JOURNAL; QUESTIONNAIRE; ADOLESCENT; ADULT; ARTICLE; CHILD; DIET THERAPY; ENZYME ASSAY; FEMALE; FERTILITY; FOLLOW UP; GENETIC SCREENING; GENETICS; INFANT; LENS SUBLUXATION; MALE; MENTAL DEFICIENCY; NEWBORN; NUTRITIONAL DEFICIENCY; OSTEOPOROSIS; PREGNANCY; PREGNANCY COMPLICATION; PRESCHOOL CHILD; SEIZURE; THROMBOEMBOLISM;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; CYSTATHIONINE BETA-SYNTHASE; ENZYME TESTS; FEMALE; FERTILITY; FOLLOW-UP STUDIES; GENETIC SCREENING; HOMOCYSTINURIA; HUMAN; INFANT; INFANT, NEWBORN; LENS SUBLUXATION; MALE; MENTAL RETARDATION; METHIONINE; OSTEOPOROSIS; PREGNANCY; PREGNANCY COMPLICATIONS; PYRIDOXINE; QUESTIONNAIRES; SEIZURES; THROMBOEMBOLISM;

EID: 0021894152     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: None

References (0)