Novel CDH3 mutations in hypotrichosis with juvenile macular dystrophy

Clinical and Experimental Dermatology

Volumn 32, Issue 2, 2007, Pages 191-196

  Indelman, M ^a   Eason, J ^b   Hummel, M ^c   Loza, O ^a   Suri, M ^d   Leys, M J ^c   Bayne, M ^e   Schwartz, F L ^e   Sprecher, E ^a,f  

^a RAMBAM MEDICAL CENTER   (Israel)

^b UNIVERSITY OF NOTTINGHAM   (United Kingdom)

^c WEST VIRGINIA UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d NOTTINGHAM UNIVERSITY HOSPITALS NHS TRUST   (United Kingdom)

^e OHIO UNIVERSITY   (United States)

^f TECHNION ISRAEL INSTITUTE OF TECHNOLOGY   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

CADHERIN; P CADHERIN; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; CDH3 GENE; FEMALE; GENE; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; HETEROZYGOSITY; HUMAN; HYPOTRICHOSIS; HYPOTRICHOSIS WITH JUVENILE MACULAR DYSTROPHY; MALE; MISSENSE MUTATION; MUTAGENESIS; NONSENSE MUTATION; PRIORITY JOURNAL; RETINA MACULA DEGENERATION; SCHOOL CHILD; VISUAL ACUITY; VISUAL IMPAIRMENT;

ADOLESCENT; CADHERINS; CHILD; CORNEAL DYSTROPHIES, HEREDITARY; DNA MUTATIONAL ANALYSIS; FEMALE; HETEROZYGOTE; HUMANS; HYPOTRICHOSIS; MALE; MOLECULAR SEQUENCE DATA; MUTATION, MISSENSE;

EID: 33846939818     PISSN: 03076938     EISSN: 13652230     Source Type: Journal    
DOI: 10.1111/j.1365-2230.2006.02335.x     Document Type: Article

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