Identification of three novel mutations in the MYO7A gene.

Human mutation

Volumn 14, Issue 2, 1999, Pages 181-

  Cuevas, J M ^a   Espinos C ^a   Millan J M ^a   Sanchez F ^a   Trujillo, M J ^a   Ayuso, C ^a   Beneyto, M ^a   Najera C ^a  

^a UNIVERSITY OF VALENCIA   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

DYNEIN ADENOSINE TRIPHOSPHATASE; MYOSIN; MYOSIN VIIA;

ARTICLE; CHROMOSOME 11; FEMALE; GENETICS; HUMAN; MALE; MUTATION; NUCLEOTIDE SEQUENCE; PEDIGREE; PERCEPTION DEAFNESS; PHENOTYPE; RETINITIS PIGMENTOSA; SINGLE STRAND CONFORMATION POLYMORPHISM; SYNDROME;

BASE SEQUENCE; CHROMOSOMES, HUMAN, PAIR 11; DYNEIN ATPASE; FEMALE; HEARING LOSS, SENSORINEURAL; HUMANS; MALE; MUTATION; MYOSINS; PEDIGREE; PHENOTYPE; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; RETINITIS PIGMENTOSA; SYNDROME;

EID: 0033584286     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/(SICI)1098-1004(1999)14:2<181::AID-HUMU11>3.0.CO;2-3     Document Type: Article

References (0)