Two novel mutations in the retinitis pigmentosa GTPase regulator (RPGR) gene in X-linked retinitis pigmentosa (RP3). Mutations in brief no. 172. Online.

M G Miano,D Valverde, T Solans, B Grammatico,C Migliaccio,V Cirigliano, C DeBernardo,V Ventruto, T Meitinger, A Wright, G Del Porto,M Baiget, M D'Urso,A Ciccodicola

Human mutation(1998)

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摘要
Recently a new gene called RPGR (retinitis pigmentosa GTPase regulator) was isolated in Xp21.1 and found to be mutated in patients with RP3 type X-linked retinitis pigmentosa. Two new mutations, the first a single base pair deletion and the other a two base pairs deletion, have been found in one Spanish and one Italian family.
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