Retinitis Pigmentosa, X-Linked, and Sinorespiratory Infections, With or Without Deafness
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-319-66816-1_635-1
Reference4 articles.
1. Heckenlively JR, Yoser SL, Friedman LH, Oversier JJ (1988) Clinical findings and common symptoms in retinitis pigmentosa. Am J Ophthalmol 105(5):504–511
2. Moore A, Escudier E, Roger G, Tamalet A, Pelosse B, Marlin S, Clément A, Geremek M, Delaisi B, Bridoux A-M, Coste A (2005) RPGR is mutated in patients with a complex X linked phenotype combining primary ciliary dyskinesia and retinitis pigmentosa. J Med Genet 43(4):326–33
3. van Dorp DB, Wright AF, Carothers AD, Bleeker-Wagemakers EM (1992) A family with RP3 type of X-linked retinitis pigmentosa: an association with ciliary abnormalities. Hum Genet 88:331–334
4. Zito I, Downes S, Patel R, Cheetham M, Ebenezer N, Jenkins S, Bhattacharya S, Webster A, Holder G, Bird A (2003) RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infections. J Med Genet 40(8):609–615
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