Linkage studies in erythrokeratodermias: Fine mapping, genetic heterogeneity, and analysis of candidate genes

Journal of Investigative Dermatology

Volumn 109, Issue 5, 1997, Pages 666-671

  Richard, Gabriela ^a,i   Lin, Jing Ping ^a   Smith, Lisa ^a   Whyte, Yolanda M ^a   Itin, Peter ^c   Wollina, Uwe ^d   Epstein Jr , Ervin ^e   Hohl, Daniel ^f   Giroux, Jean Mario ^g   Charnas, Lawrence ^h   Bale, Sherri J ^a   DiGiovanna, John J ^b,j  

^a Laboratory of Skin Biology   (United States)

^b NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES   (United States)

^c UNIVERSITY OF BASEL   (Switzerland)

^d FRIEDRICH SCHILLER UNIVERSITY JENA   (Germany)

^e UNIVERSITY OF CALIFORNIA   (United States)

^f Children's Hospital Lausanne   (Switzerland)

^g UNIVERSITÉ DE MONTRÉAL   (Canada)

^h EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH AND HUMAN DEVELOPMENT   (United States)

ⁱ Brown University School of Medicine ^*  (United States)

^j BROWN UNIVERSITY   (United States)

more..

Author keywords

Ataxia; Chromosome 1; Connexin; Erythrokeratodermia variabilis; Greither disease

Indexed keywords

GAP JUNCTION PROTEIN;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 1P; CLINICAL ARTICLE; ERYTHEMA; FEMALE; GENE LOCATION; GENETIC HETEROGENEITY; GENETIC LINKAGE; HUMAN; HYPERKERATOSIS; MALE; PATHOGENESIS; PRIORITY JOURNAL;

EID: 9844222499     PISSN: 0022202X     EISSN: None     Source Type: Journal    
DOI: 10.1111/1523-1747.ep12337713     Document Type: Article

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