Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2

Genomics

Volumn 61, Issue 3, 1999, Pages 243-258

  Liang, Yong ^a,b   Wang, Aihui ^a,b   Belyantseva, Inna A ^a   Anderson, David W ^a   Probst, Frank J ^c   Barber, Thomas D ^a,b   Miller, Webb ^d   Touchman, Jeffrey W ^e   Jin, Long ^f   Sullivan, Susan L ^e   Sellers, James R ^g   Camper, Sally A ^d   Lloyd, Ricardo V ^f   Kachar, Bechara ^a   Friedman, Thomas B ^a   Fridell, Robert A ^a  

^a NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS   (United States)

^b MICHIGAN STATE UNIVERSITY   (United States)

^c UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

^d The Pennsylvania State University   (United States)

^e NATIONAL INSTITUTES OF HEALTH   (United States)

^f MAYO CLINIC   (United States)

^g NATIONAL HEART LUNG AND BLOOD INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MYOSIN; MYOSIN XV; UNCLASSIFIED DRUG;

ANIMAL TISSUE; ARTICLE; CHROMOSOME 11; CHROMOSOME 17P; CONGENITAL DEAFNESS; CORTI ORGAN; DNA SEQUENCE; HAIR CELL; HUMAN; HUMAN TISSUE; HYPOPHYSIS; IMMUNOHISTOCHEMISTRY; IN SITU HYBRIDIZATION; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN EXPRESSION;

EID: 0032729835     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1999.5976     Document Type: Article

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