Null alleles of the COL5A1 gene of type V collagen are a cause of the classical forms of ehlers-danlos syndrome (types I and II)

American Journal of Human Genetics

Volumn 66, Issue 6, 2000, Pages 1757-1765

  Schwarze, Ulrike ^a   Atkinson, Mary ^a   Hoffman, Guy G ^b   Greenspan, Daniel S ^b   Byers, Peter H ^a  

^a UNIVERSITY OF WASHINGTON   (United States)

^b UNIVERSITY OF WISCONSIN SCHOOL OF MEDICINE AND PUBLIC HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COLLAGEN TYPE 5; TENASCIN;

ADOLESCENT; ARTICLE; CHILD; CHROMOSOME 9Q; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DNA POLYMORPHISM; DNA SEQUENCE; EHLERS DANLOS SYNDROME; FEMALE; GENE; GENE MUTATION; GENETIC ANALYSIS; GENETIC HETEROGENEITY; HUMAN; MALE; PRIORITY JOURNAL;

EID: 0033910981     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302933     Document Type: Article

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