A new familial syndrome characterized by pigmentary retinopathy, hypogonadism, mental retardation, nerve deafness and glucose intolerance
(Q56592902)
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A new familial syndrome characterized by pigmentary retinopathy, hypogonadism, mental retardation, nerve deafness and glucose intolerance
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(Q13442814)
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| (P304) |
23-32
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(Q1860)
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1
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| (P478) |
60
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| (P577) |
+1976-01-00T00:00:00Z
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| (P921) |
(Q37525)
(Q938107)
(Q2661464)
(Q18967037)
(Q12133)
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| (P1433) |
(Q2842959)
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| (P1476) |
"A new familial syndrome characterized by pigmentary retinopathy, hypogonadism, mental retardation, nerve deafness and glucose intolerance" (language: en)
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| (P2093) |
John A. Edwards
Prahlad K. Sethi
Andrew J. Scoma
Robin M. Bannerman
Lawrence A. Frohman
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