(Q34559746)
Statements
RPGR is mutated in patients with a complex X linked phenotype combining primary ciliary dyskinesia and retinitis pigmentosa (English)
A Moore
E Escudier
G Roger
A Tamalet
B Pelosse
S Marlin
A Clément
M Geremek
B Delaisi
A-M Bridoux
M Witt
B Duriez
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