Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bβ

Cell

Volumn 105, Issue 5, 2001, Pages 587-597

  Zhao, Chunjie ^a   Takita, Junko ^b   Tanaka, Yosuke ^a   Setou, Mitsutoshi ^a   Nakagawa, Terunaga ^a   Takeda, Sen ^a   Yang, Hong Wei ^a   Terada, Sumio ^a   Nakata, Takao ^a   Takei, Yosuke ^a   Saito, Masaaki ^c   Tsuji, Shoji ^c   Hayashi, Yasuhide ^b   Hirokawa, Nobutaka ^a  

^a UNIVERSITY OF TOKYO   (Japan)

^b UNIVERSITY OF TOKYO   (Japan)

^c NIIGATA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

KINESIN; MICROTUBULE PROTEIN; PROTEIN KIF1BBETA; PROTIEN KIF1B; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL MODEL; ANIMAL TISSUE; APNEA; ARTICLE; BINDING SITE; CONTROLLED STUDY; DISEASE CLASSIFICATION; GENE MUTATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HETEROZYGOTE; HUMAN; HUMAN CELL; KNOCKOUT MOUSE; MOUSE; MUSCLE WEAKNESS; NERVE CELL CULTURE; NERVE CELL NECROSIS; NERVE FIBER TRANSPORT; NONHUMAN; PERIPHERAL NEUROPATHY; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN EXPRESSION; PROTEIN FAMILY; PROTEIN TRANSPORT; SYNAPSE VESICLE;

ANIMALIA;

EID: 0035369084     PISSN: 00928674     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0092-8674(01)00363-4     Document Type: Article

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