A novel mutation in the CFTR gene correlates with severe clinical phenotype in seven Hispanic patients

Journal of Medical Genetics

Volumn 37, Issue 3, 2000, Pages 215-218

  Wang, J ^a   Bowman, M C ^a   Hsu, E ^a   Wertz, K ^a   Wong, L J C ^a  

^a GEORGETOWN UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSMEMBRANE CONDUCTANCE REGULATOR;

CYSTIC FIBROSIS; DISEASE SEVERITY; ETHNIC GROUP; GENE MUTATION; HUMAN; LETTER; PHENOTYPE; PRIORITY JOURNAL;

EID: 0034014387     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.37.3.215     Document Type: Letter

References (23)