KCNE1-like gene is deleted in ACME contiguous gene syndrome: Identification and characterization of the human and mouse homologs

Genomics

Volumn 60, Issue 3, 1999, Pages 251-257

  Piccini, Monica ^a   Vitelli, Francesca ^a   Seri, Marco ^b   Galietta, Luis J V ^b   Moran, Oscar ^c   Bulfone, Alessandro ^d   Banfi, Sandro ^d   Pober, Barbara ^e   Renieri, Alessandra ^a  

^a UNIVERSITY HOSPITAL OF SIENA   (Italy)

^b G GASLINI INSTITUTE   (Italy)

^c CNR   (Italy)

^d TELETHON INSTITUTE OF GENETICS AND MEDICINE TIGEM   (Italy)

^e YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; COMPLEMENTARY DNA;

ALPORT SYNDROME; ARTICLE; DNA LIBRARY; ELLIPTOCYTOSIS; EMBRYO DEVELOPMENT; GENE DELETION; GENE EXPRESSION; GENETIC ANALYSIS; HUMAN; MALE; MENTAL DEFICIENCY; MIDFACE HYPOPLASIA; MOUSE; NONHUMAN; OPEN READING FRAME; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN FAMILY; SEQUENCE HOMOLOGY;

MUSTELA VISON; RODENTIA;

EID: 0033568148     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1999.5904     Document Type: Article

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