Acral self-healing collodion baby: Report of a new clinical phenotype caused by a novel TGM1 mutation

British Journal of Dermatology

Volumn 161, Issue 2, 2009, Pages 456-463

  Mazereeuw Hautier, J ^a   Aufenvenne, K ^b   Deraison, C ^a,c   Ahvazi, B ^d   Oji, V ^b   Traupe, H ^b   Hovnanian, A ^a  

^a CHU PURPAN   (France)

^b UNIVERSITY OF MÜNSTER   (Germany)

^c INSERM   (France)

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

Author keywords

Ichthyosis; Self healing collodion baby; Transglutaminase 1

Indexed keywords

PROTEIN GLUTAMINE GAMMA GLUTAMYLTRANSFERASE; TRANSGLUTAMINASE 1;

ARTICLE; CASE REPORT; FEMALE; FINGER; GENE DELETION; GENETIC PREDISPOSITION; GENETICS; HETEROZYGOTE; HUMAN; ICHTHYOSIS; NEWBORN; PHENOTYPE; REMISSION; TOE;

FEMALE; FINGERS; GENETIC PREDISPOSITION TO DISEASE; HETEROZYGOTE; HUMANS; ICHTHYOSIS; INFANT, NEWBORN; PHENOTYPE; REMISSION, SPONTANEOUS; SEQUENCE DELETION; TOES; TRANSGLUTAMINASES;

EID: 73349108452     PISSN: 00070963     EISSN: 13652133     Source Type: Journal    
DOI: 10.1111/j.1365-2133.2009.09277.x     Document Type: Article

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