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Pediatrics International

Volumn 53, Issue 1, 2011, Pages 107-110

A case of progressive familial intrahepatic cholestasis type 1 with compound heterozygous mutations of ATP8B1

(5) Numakura, Chikahiko a Abukawa, Daiki b Kimura, Toshiyuki c Tanabe, Saori c Hayasaka, Kiyoshi a

a YAMAGATA UNIVERSITY (Japan)

b MIYAGI CHILDREN S HOSPITAL (Japan)

c Department of Pediatrics (Japan)

Author keywords

ATP8B1; familial intrahepatic cholestasis 1; FIC1; progressive familial intrahepatic cholestasis

Indexed keywords

ALPHA TOCOPHEROL; CALCIUM LACTATE; COLESTILAN; HYDROXYZINE; LIPOPROTEIN X; URSODEOXYCHOLIC ACID; VITAMIN D; VITAMIN K GROUP;

ARTICLE; ATP8B1 GENE; CASE REPORT; CHILD; CLINICAL FEATURE; FEMALE; GENE; GENE DELETION; GENE SEQUENCE; GENOTYPE PHENOTYPE CORRELATION; HETEROZYGOSITY; HUMAN; HYPERBILIRUBINEMIA; INTRAHEPATIC CHOLESTASIS; JAUNDICE; NUCLEOTIDE SEQUENCE; PRESCHOOL CHILD; PRIORITY JOURNAL; PROGRESSIVE FAMILIAL INTRAHEPATIC CHOLESTASIS TYPE 1; PRURITUS; RICKETS; SEQUENCE ANALYSIS; SYMPTOM;

ADENOSINE TRIPHOSPHATASES; CHILD, PRESCHOOL; CHOLESTASIS, INTRAHEPATIC; FEMALE; HETEROZYGOTE; HUMANS; MUTATION;

EID: 79951979886 PISSN: 13288067 EISSN: 1442200X Source Type: Journal
DOI: 10.1111/j.1442-200X.2010.03238.x Document Type: Article

Times cited : (6)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.