Cutting edge genetic studies in primary ciliary dyskinesia

Thorax

Volumn 67, Issue 5, 2012, Pages 464-

  Knowles, Michael R ^a   Leigh, Margaret W ^a   Zariwala, Maimoona A ^a  

^a UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANALYTIC METHOD; CILIARY DYSKINESIA; DIAGNOSTIC TEST; GENETIC SCREENING; GENETICS; LETTER; PREDICTION; PRIORITY JOURNAL;

EID: 84859819522     PISSN: 00406376     EISSN: 14683296     Source Type: Journal    
DOI: 10.1136/thoraxjnl-2012-201609     Document Type: Letter

References (2)

1. Knowles MR, Leigh MW, Carson JL, et al. Mutations of DNAH11 in primary ciliary dyskinesia patients with normal ciliary ultrastructure. Thorax 2012;67:433-41.
2. Hogg C, Bush A. Genotyping in primary ciliary dyskinesia: ready for prime time, or a fringe benefit? Thorax 2012;67:377-8.