SCOPUS 정보 검색 플랫폼

Volumn 77, Issue 4, 1997, Pages 369-370

Absence of mutations in the regulatory domain of the gap junction protein connexin 43 in patients with visceroatrial heterotaxy

(4) Splitt, Miranda Penman a,b Tsai, Meng Y a Burn, John a Goodship, Judith A a

a NEWCASTLE UNIVERSITY (United Kingdom)

b Department of Human Genetics ^* (United Kingdom)

Author keywords

Asplenia; Connexin 43; Isomerism sequence; Polysplenia; Visceroatrial heterotaxy

Indexed keywords

CONNEXIN 43;

ACCESSORY SPLEEN; ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; CONGENITAL HEART MALFORMATION; HEART ATRIUM SEPTUM DEFECT; HUMAN; MUTATION; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROTEIN PHOSPHORYLATION;

EID: 0004600209 PISSN: 13556037 EISSN: None Source Type: Journal
DOI: 10.1136/hrt.77.4.369 Document Type: Article

Times cited : (29)

References (9)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.