Genotype-phenotype correlations of KCNJ2 mutations in Japanese patients with Andersen-Tawil syndrome.

Human mutation

Volumn 28, Issue 2, 2007, Pages 208-

  Haruna, Yoshisumi ^a   Kobori, Atsushi ^a   Makiyama, Takeru ^a   Yoshida, Hidetada ^a   Akao, Masaharu ^a   Doi, Takahiro ^a   Tsuji, Keiko ^a   Ono, Seiko ^a   Nishio, Yukiko ^a   Shimizu, Wataru ^a   Inoue, Takehiko ^a   Murakami, Tomoaki ^a   Tsuboi, Naoya ^a   Yamanouchi, Hideo ^a   Ushinohama, Hiroya ^a   Nakamura, Yoshihide ^a   Yoshinaga, Masao ^a   Horigome, Hitoshi ^a   Aizawa, Yoshifusa ^a   Kita, Toru ^a   Horie, Minoru ^a   more..

^a KYOTO UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

INWARDLY RECTIFYING POTASSIUM CHANNEL; KCNJ2 PROTEIN, HUMAN; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; AGED; ANDERSEN SYNDROME; ANIMAL; ARTICLE; CELL STRAIN COS1; CERCOPITHECUS; CHEMISTRY; CHILD; ECHOCARDIOGRAPHY; ECHOGRAPHY; FEMALE; GENETICS; GENOTYPE; HEART VENTRICLE TACHYCARDIA; HUMAN; MALE; MIDDLE AGED; MUTATION; NUCLEOTIDE SEQUENCE; PATCH CLAMP; PERIODIC PARALYSIS; PHENOTYPE; PHYSIOLOGY; PRESCHOOL CHILD; PROTEIN TERTIARY STRUCTURE;

ADOLESCENT; ADULT; AGED; ANDERSEN SYNDROME; ANIMALS; CERCOPITHECUS AETHIOPS; CHILD; CHILD, PRESCHOOL; COS CELLS; DNA MUTATIONAL ANALYSIS; ECHOCARDIOGRAPHY; FEMALE; GENOTYPE; HUMANS; MALE; MIDDLE AGED; MUTATION; PARALYSES, FAMILIAL PERIODIC; PATCH-CLAMP TECHNIQUES; PHENOTYPE; POTASSIUM CHANNELS, INWARDLY RECTIFYING; PROTEIN STRUCTURE, TERTIARY; TACHYCARDIA, VENTRICULAR;

EID: 33847710335     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9483     Document Type: Article

References (0)