Truncating variants in the majority of the cytoplasmic domain of pcdh15 are unlikely to cause usher syndrome 1F

Journal of Molecular Diagnostics

Volumn 16, Issue 6, 2014, Pages 673-678

  Perreault Micale, Cynthia ^a   Frieden, Alexander ^a   Kennedy, Caleb J ^a   Neitzel, Dana ^a   Sullivan, Jessica ^a   Faulkner, Nicole ^a   Hallam, Stephanie ^a   Greger, Valerie ^a  

^a Good Start Genetics Inc ^*  (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AFRICAN AMERICAN; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; DNA SEQUENCE; EXON; GENE; GENE FREQUENCY; GENE SEQUENCE; GENETIC VARIABILITY; HETEROZYGOTE; HUMAN; INTRON; MAJOR CLINICAL STUDY; NUCLEOTIDE SEQUENCE; PCDH15 GENE; PROTEIN STRUCTURE; USHER SYNDROME TYPE 1F; CYTOPLASM; GENETICS; METABOLISM; POLYMERASE CHAIN REACTION; USHER SYNDROME;

CADHERIN; PCDH15 PROTEIN, HUMAN;

CADHERINS; CYTOPLASM; HUMANS; POLYMERASE CHAIN REACTION; USHER SYNDROMES;

EID: 84908100929     PISSN: 15251578     EISSN: 19437811     Source Type: Journal    
DOI: 10.1016/j.jmoldx.2014.07.001     Document Type: Article

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