(Q51936807)
Statements
Novel exon 1 mutations in MECP2 implicate isoform MeCP2_e1 in classical Rett syndrome. (English)
1 reference
Carol J Saunders
1 reference
Berge E Minassian
1 reference
Eva W C Chow
1 reference
Weiwei Zhao
1 reference
John B Vincent
1 reference
1 May 2009
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149A
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5
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1019-1023
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Identifiers
1 reference