Mutations in the CACNA1F and NYX genes in British CSNBX families.

Human mutation

Volumn 21, Issue 2, 2003, Pages 169-

  Zito, Ilaria ^a   Allen, Louise E ^a   Patel, Reshma J ^a   Meindl, Alfons ^a   Bradshaw, Keith ^a   Yates, John R ^a   Bird, Alan C ^a   Erskine, Lynda ^a   Cheetham, Michael E ^a   Webster, Andrew R ^a   Poopalasundaram, Subathra ^a   Moore, Anthony T ^a   Trump, Dorothy ^a   Hardcastle, Alison J ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CACNA1F PROTEIN, HUMAN; CALCIUM CHANNEL; CALCIUM CHANNEL L TYPE; NYX PROTEIN, HUMAN; PROTEOGLYCAN;

ARTICLE; CHEMISTRY; CLINICAL TRIAL; EXON; FEMALE; FOUNDER EFFECT; GENETICS; HUMAN; LEUKOCYTE; MALE; MULTICENTER STUDY; MUTATION; NIGHT BLINDNESS; NUCLEOTIDE SEQUENCE; PEDIGREE; UNITED KINGDOM; X CHROMOSOME LINKED DISORDER;

CALCIUM CHANNELS; CALCIUM CHANNELS, L-TYPE; DNA MUTATIONAL ANALYSIS; EXONS; FEMALE; FOUNDER EFFECT; GENETIC DISEASES, X-LINKED; GREAT BRITAIN; HUMANS; LEUKOCYTES; MALE; MUTATION; NIGHT BLINDNESS; PEDIGREE; PROTEOGLYCANS;

EID: 0037316093     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9106     Document Type: Article

References (0)