The spectrum of mutations causing end-plate acetylcholinesterase deficiency

Annals of Neurology

Volumn 47, Issue 2, 2000, Pages 162-170

  Ohno, Kinji ^a   Engel, Andrew G ^a   Brengman, Joan M ^a   Shen, Xin Ming ^a   Heidenreich, Fedor ^b   Vincent, Angela ^c   Milone, Margherita ^a   Tan, Ersin ^d   Demitci, Mehmet ^d   Walsh, Peter ^e   Nakano, Satoshi ^f   Akiguchi, Ichiro ^f  

^a MAYO CLINIC   (United States)

^b HANNOVER MEDICAL SCHOOL   (Germany)

^c UNIVERSITY OF OXFORD   (United Kingdom)

^d HACETTEPE UNIVERSITY   (Turkey)

^e PRINCESS MARGARET HOSPITAL FOR CHILDREN   (Australia)

^f KYOTO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLCHOLINESTERASE;

ANIMAL CELL; ARTICLE; CARBOXY TERMINAL SEQUENCE; CLINICAL ARTICLE; ENZYME DEFICIENCY; FEMALE; GENE MUTATION; GENETIC ENGINEERING; HUMAN; MALE; MISSENSE MUTATION; NERVE ENDING; NONHUMAN; PRIORITY JOURNAL;

ACETYLCHOLINESTERASE; ADOLESCENT; ADULT; ANIMALS; COLLAGEN; COS CELLS; DNA MUTATIONAL ANALYSIS; FEMALE; GENE EXPRESSION; HUMANS; INFANT; MALE; MICROSCOPY, ELECTRON; MOTOR ENDPLATE; MUSCLE PROTEINS; MUTATION; MUTATION, MISSENSE;

EID: 17344391484     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/1531-8249(200002)47:2<162::AID-ANA5>3.0.CO;2-Q     Document Type: Article

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