Intragenic telSMN mutations: frequency, distribution, evidence of a founder effect, and modification of the spinal muscular atrophy phenotype by cenSMN copy number. (Q24539804)
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(P50) (Q58635204)
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(P304) 1712-1723
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(P433) 6
(P478) 63
(P577) Tuesday, December 1, 1998
(P921) (Q580290)
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(P1476) "Intragenic telSMN mutations: frequency, distribution, evidence of a founder effect, and modification of the spinal muscular atrophy phenotype by cenSMN copy number" (language: en)
(P2093) Parsons DW
McAndrew PE
Mendell JR
Prior TW
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