SCOPUS 정보 검색 플랫폼

Volumn 68, Issue 3, 2001, Pages 753-758

Familial dysautonomia is caused by mutations of the IKAP gene

(8) Anderson, Sylvia L a Coli, Rocco a Daly, Ira W a Kichula, Elizabeth A a Rork, Matthew J a Volpi, Sabrina A a Ekstein, Josef b Rubin, Berish Y a

a FORDHAM UNIVERSITY (United States)

b Dor Yeshorim (United States)

Author keywords

[No Author keywords available]

Indexed keywords

I KAPPA B; PROTEIN SERINE THREONINE KINASE; RNA;

ARTICLE; CHROMOSOME 9Q; CHROMOSOME MAP; DYSAUTONOMIA; ENZYME PHOSPHORYLATION; EXON; GENE MUTATION; HAPLOTYPE; HOMOZYGOSITY; HUMAN; INTRON; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SEQUENCE ANALYSIS;

EID: 0035097484 PISSN: 00029297 EISSN: None Source Type: Journal
DOI: 10.1086/318808 Document Type: Article

Times cited : (373)

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