Intragenic loss of function mutations demonstrate the primary role of FMR1 in fragile X syndrome (Q41315849)
scientific article published on August 1, 1995
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(P31) (Q13442814)
(P304) 483-485
(P407) (Q1860)
(P433) 4
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(P577) Tuesday, August 1, 1995
(P921) (Q221472)
(P953) http://www.nature.com/articles/ng0895-483
http://www.nature.com/articles/ng0895-483.pdf
(P1433) (Q976454)
(P1476) "Intragenic loss of function mutations demonstrate the primary role of FMR1 in fragile X syndrome" (language: en)
(P2093) K. A. Lugenbeel
A. M. Peier
N. L. Carson
A. E. Chudley
D. L. Nelson
(P2860) (Q41669091)
(Q28270283)
(Q38317052)
(Q52042510)
(Q35643836)
(Q28117885)
(Q41579799)
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(Q40811458)
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(Q72706845)
(Q52024856)
(Q48079766)
(Q34332608)
(Q95821195)
(Q24311412)
(Q72586891)
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(Q42623011)
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description scientific article published on August 1, 1995

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