A unique exonic splice enhancer mutation in a family with X-linked mental retardation and epilepsy points to a novel role of the renin receptor (Q24297376)
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Current Data About A unique exonic splice enhancer mutation in a family with X-linked mental retardation and epilepsy points to a novel role of the renin receptor
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(P1932) Alfons Meindl

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(P1932) Juliane Ramser

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(P1476) "A unique exonic splice enhancer mutation in a family with X-linked mental retardation and epilepsy points to a novel role of the renin receptor" (language: en)

(P2093) Fatima E Abidi
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Celine A Burckle
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Claus Lenski
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Helga Toriello
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Gaiping Wen
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Herbert A Lubs
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Stefanie Engert
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Roger E Stevenson
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Charles E Schwartz
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Genevieve Nguyen
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External Links
(P356) 10.1093/HMG/DDI094
(P698) 15746149
(P3181) 1987419
(P5875) 7988255