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Volumn 36, Issue 1, 1997, Pages 9-13

Familial Hypocholinesterasemia Found in a Family and a New Confirmed Mutation

Author keywords

Cholinesterase; Gene analysis; Point mutation

Indexed keywords

CHOLINESTERASE; DNA; PRIMER DNA;

EID: 0030639996     PISSN: 09182918     EISSN: None     Source Type: Journal    
DOI: 10.2169/internalmedicine.36.9     Document Type: Article
Times cited : (11)

References (13)
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  • 3
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  • 4
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    • Inactivation of the cholinesterase gene by Alu insertion: Possible mechanism for human gene transposition
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  • 5
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    • DNA mutations associated with the human butyrylcholinesterase J-variant
    • Bartels CF, James K, La Du BN. DNA mutations associated with the human butyrylcholinesterase J-variant. Am J Hum Genet 50: 1104, 1992.
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    • A variant serum cholinesterase and a confirmed point mutation at Gly-365 to Arg found in a patient with liver cirrhosis
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    • Genetic basis of the silent phenotype of serum butyrylcholinesterase in three compound heterozygotes
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  • 8
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    • A method for the detection of atypical forms of human cholinesterase. Determination of dibucaine numbers
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  • 11
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    • A polymorphism (K variant?) of human serum cholinesterase at nucleotide 1615, coding for Ala/Thr 539
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.