RGD Reference Report - A recurrent intragenic deletion mutation in DSG4 gene in three Pakistani families with autosomal recessive hypotrichosis. - Rat Genome Database

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A recurrent intragenic deletion mutation in DSG4 gene in three Pakistani families with autosomal recessive hypotrichosis.

Authors: Rafiq, MA  Ansar, M  Mahmood, S  Haque, S  Faiyaz-ul-Haque, M  Leal, SM  Ahmad, W 
Citation: Rafiq MA, etal., J Invest Dermatol. 2004 Jul;123(1):247-8.
RGD ID: 1599796
Pubmed: PMID:15191570   (View Abstract at PubMed)
PMCID: PMC6157275   (View Article at PubMed Central)
DOI: DOI:10.1111/j.0022-202X.2004.22715.x   (Journal Full-text)

Abstract for this paper unavailable



RGD Manual Disease Annotations    Click to see Annotation Detail View

  
Object SymbolSpeciesTermQualifierEvidenceWithNotesSourceOriginal Reference(s)
DSG4Humanhypotrichosis  IAGP DNA:deletionRGD 
Dsg4Rathypotrichosis  ISODSG4 (Homo sapiens)DNA:deletionRGD 
Dsg4Mousehypotrichosis  ISODSG4 (Homo sapiens)DNA:deletionRGD 

Objects Annotated

Genes (Rattus norvegicus)
Dsg4  (desmoglein 4)

Genes (Mus musculus)
Dsg4  (desmoglein 4)

Genes (Homo sapiens)
DSG4  (desmoglein 4)


Additional Information