Mutations in transglutaminase 1 gene in autosomal recessive congenital ichthyosis in Egyptian families

Disease Markers

Volumn 20, Issue 6, 2004, Pages 325-332

  Shawky, R M ^a   Sayed, N S ^a   Elhawary, N A ^a  

^a AIN SHAMS UNIVERSITY   (Egypt)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN GLUTAMINE GAMMA GLUTAMYLTRANSFERASE;

ADOLESCENT; ADULT; ALLELE; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHILD; CLINICAL ARTICLE; CONGENITAL ICHTHYOSIFORM ERYTHRODERMA; CONTROLLED STUDY; CORRELATION ANALYSIS; EGYPT; EXON; FEMALE; GENE FREQUENCY; GENE MUTATION; GENETIC ANALYSIS; GENOTYPE; HUMAN; HYBRID; INTRON; MALE; NEWBORN; PHENOTYPE; PRIORITY JOURNAL;

EID: 15244339432     PISSN: 02780240     EISSN: None     Source Type: Journal    
DOI: 10.1155/2004/965968     Document Type: Article

References (28)

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