TRPM1 mutations are associated with the complete form of congenital stationary night blindness

Molecular Vision

Volumn 16, Issue , 2010, Pages 425-437

  Nakamura, Makoto ^a   Sanuki, Rikako ^b,c   Yasuma, Tetsuhiro R ^a   Onishi, Akishi ^b,c   Nishiguchi, Koji M ^a   Koike, Chieko ^b,c   Kadowaki, Mikiko ^b   Kondo, Mineo ^a   Miyake, Yozo ^a,d   Furukawa, Takahisa ^b,c  

^a NAGOYA UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^b OSAKA BIOSCIENCE INSTITUTE   (Japan)

^c JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

^d AICHI SHUKUTOKU UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

GLUTAMATE RECEPTOR; METABOTROPIC RECEPTOR 6; NYCTALOPIN; PROTEIN; TRANSIENT RECEPTOR POTENTIAL CHANNEL M1; UNCLASSIFIED DRUG; TRANSIENT RECEPTOR POTENTIAL CHANNEL M; TRPM1 PROTEIN, HUMAN; TRPM1 PROTEIN, MOUSE;

A WAVE; ADULT; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; B WAVE; BIOMICROSCOPY; CASE REPORT; COLOR VISION TEST; CONGENITAL BLINDNESS; CONTROLLED STUDY; DISEASE ASSOCIATION; ELECTRORETINOGRAPHY; EXON; EYE PHOTOGRAPHY; EYE REFRACTION; GENE SEQUENCE; HETEROZYGOTE; HUMAN; INTRON; JAPANESE; MALE; MISSENSE MUTATION; MOUSE; MYOPIA; NIGHT BLINDNESS; NONHUMAN; NUCLEOTIDE SEQUENCE; OPHTHALMOSCOPY; PERIMETRY; PRIORITY JOURNAL; PROTEIN LOCALIZATION; PROTEIN SYNTHESIS; RETINA BIPOLAR GANGLION CELL; VISUAL ACUITY; VISUAL SYSTEM EXAMINATION; ANIMAL; CELL LINE; CHILD; FEMALE; GENETIC PREDISPOSITION; GENETICS; INTRACELLULAR SPACE; METABOLISM; MOLECULAR GENETICS; MOUSE MUTANT; MUTATION; PEDIGREE; PROTEIN TRANSPORT;

ADULT; ANIMALS; BASE SEQUENCE; CELL LINE; CHILD; DNA MUTATIONAL ANALYSIS; ELECTRORETINOGRAPHY; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HETEROZYGOTE; HUMANS; INTRACELLULAR SPACE; MALE; MICE; MICE, KNOCKOUT; MOLECULAR SEQUENCE DATA; MUTATION; MUTATION, MISSENSE; NIGHT BLINDNESS; PEDIGREE; PROTEIN TRANSPORT; TRPM CATION CHANNELS; YOUNG ADULT;

EID: 77952315144     PISSN: None     EISSN: 10900535     Source Type: Journal    
DOI: None     Document Type: Article

References (44)

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