Juvenile hyaline fibromatosis and infantile systemic hyalinosis overlap associated with a novel mutation in capillary morphogenesis protein-2 gene

American Journal of Dermatopathology

Volumn 29, Issue 1, 2007, Pages 99-103

  Antaya, Richard J ^a   Cajaiba, Mariana M ^a   Madri, Joseph ^a   Lopez, Maria A ^b   Ramirez, Maria Celeste M ^c   Martignetti, John A ^c   Reyes Múgica, Miguel ^a  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b Lawrence and Memorial Hospital ^*  (United States)

^c MOUNT SINAI SCHOOL OF MEDICINE   (United States)

Author keywords

CMG2; Infantile systemic hyalinosis; Juvenile hyaline fibromatosis; Mutation

Indexed keywords

ARTICLE; CASE REPORT; CLINICAL FEATURE; DERMIS; DISABILITY; FEMALE; FIBROMATOSIS; GENE MUTATION; HUMAN; HUMAN TISSUE; MORPHOGENESIS; PATHOLOGY; PRESCHOOL CHILD; PRIORITY JOURNAL; SUBCUTANEOUS TISSUE;

ALLELES; CONNECTIVE TISSUE DISEASES; DNA; FEMALE; FIBROMA; GERM-LINE MUTATION; HUMANS; HYALIN; INFANT; MEMBRANE PROTEINS; SKIN; SKIN DISEASES;

EID: 33846853510     PISSN: 01931091     EISSN: None     Source Type: Journal    
DOI: 10.1097/01.dad.0000245636.39098.e5     Document Type: Article

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