Spectrum of CFTR mutations in Mexican cystic fibrosis patients: identification of five level mutations (W1098C, 846deIT, P750L, 4160insGGGC and 297-1G→A)

Human Genetics

Volumn 106, Issue 3, 2000, Pages 360-365

  Orozco, Lorena ^a,b   Velázquez, Rafael ^a,b   Zielenski, Julian ^c   Tsui, Lap Chee ^c   Chávez, Margarita ^a   Lezana, José Luis ^d   Saldana, Yolanda ^a,b   Hernández, Elizabeth ^a   Carnevale, Alessandra ^a  

^a INSTITUTO NACIONAL DE PEDIATRÍA   (Mexico)

^b INSTITUTO POLITÉCNICO NACIONAL   (Mexico)

^c HOSPITAL FOR SICK CHILDREN   (Canada)

^d Asoc Mexicana de Fibrosis Quistica   (Mexico)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSMEMBRANE CONDUCTANCE REGULATOR;

ADULT; ARTICLE; CHILD; CONTROLLED STUDY; CYSTIC FIBROSIS; ETHNIC GROUP; EUROPE; FAMILY; FEMALE; GENE MUTATION; GENE POOL; GENETIC ANALYSIS; GENETIC HETEROGENEITY; GENETIC SCREENING; HUMAN; HUMAN CELL; INFANT; MAJOR CLINICAL STUDY; MALE; MEXICO; MUTATION RATE; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM;

CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; FEMALE; GENE FREQUENCY; HUMANS; MALE; MEXICO; MUTATION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; VARIATION (GENETICS);

EID: 0343527249     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390051051     Document Type: Article

References (42)

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