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JMG.2005.034868
JMG.2005.034868
http://dx.doi.org/10.1136/JMG.2005.034868
RPGR is mutated in patients with a complex X linked phenotype combining primary ciliary dyskinesia and retinitis pigmentosa
P356
Q34559746-87FC4F88-6B55-4A0A-872D-1232F5064A9B
P356
JMG.2005.034868
http://dx.doi.org/10.1136/JMG.2005.034868