Molecular genetic support for the rule of dichotomy in type 2 segmental Darier disease

British Journal of Dermatology

Volumn 166, Issue 2, 2012, Pages 464-466

  Folster Holst R ^a   Nellen, R G L ^b,c   Jensen, J M ^a   Poblete Gutierrez P ^b   Steijlen, P M ^b   Schwarz, T ^a   Happle, R ^d   Van Geel, M ^b   Frank, J ^b  

^a UNIVERSITY HOSPITAL SCHLESWIG HOLSTEIN   (Germany)

^b MAASTRICHT UNIVERSITY   (Netherlands)

^c IJSSELLAND HOSPITAL   (Netherlands)

^d PHILIPPS UNIVERSITY MARBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ATP2A2 PROTEIN; GENOMIC DNA; PROTEIN; UNCLASSIFIED DRUG;

ACANTHOSIS; CASE REPORT; CHILD; DARIER DISEASE; DNA EXTRACTION; DNA ISOLATION; FAMILY HISTORY; HAPLOTYPE; HETEROZYGOSITY LOSS; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; HYPERKERATOSIS; INFANT; LETTER; MALE; MOLECULAR GENETICS; PRESCHOOL CHILD; PRIORITY JOURNAL; SEQUENCE ANALYSIS; TYPE 2 SEGMENTAL DARIER DISEASE;

DARIER DISEASE; HUMANS; INFANT; LOSS OF HETEROZYGOSITY; MALE; MUTATION, MISSENSE; PEDIGREE; SARCOPLASMIC RETICULUM CALCIUM-TRANSPORTING ATPASES;

EID: 84856187211     PISSN: 00070963     EISSN: 13652133     Source Type: Journal    
DOI: 10.1111/j.1365-2133.2011.10593.x     Document Type: Letter

References (10)

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