Spectrum of splicing errors caused by CHRNE mutations affecting introns and intron/exon boundaries.

Journal of medical genetics

Volumn 42, Issue 8, 2005, Pages

  Ohno, K ^a   Tsujino, A ^a   Shen, X M ^a   Milone, M ^a   Engel, A G ^a  

^a MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHRNE PROTEIN, HUMAN; NICOTINIC RECEPTOR;

ADULT; ALLELE; ANIMAL; ARTICLE; CELL STRAIN COS1; CERCOPITHECUS; CHILD; CONGENITAL MYASTHENIC SYNDROME; EXON; FEMALE; GENETICS; HUMAN; INTRON; MALE; MIDDLE AGED; MOLECULAR CLONING; MOLECULAR GENETICS; MUTATION; NUCLEOTIDE SEQUENCE; PRESCHOOL CHILD; RNA SPLICING;

ADULT; ALLELES; ANIMALS; BASE SEQUENCE; CERCOPITHECUS AETHIOPS; CHILD; CHILD, PRESCHOOL; CLONING, MOLECULAR; COS CELLS; EXONS; FEMALE; HUMANS; INTRONS; MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MUTATION; MYASTHENIC SYNDROMES, CONGENITAL; RECEPTORS, NICOTINIC; RNA SPLICING;

EID: 33344474514     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.2004.026682     Document Type: Article

References (0)