Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms (Q24676539)
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Current Data About Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms
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(P1476) "Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms" (language: en)

(P2093) H L Wilson
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A C C Wong
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S R Shaw
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W-Y Tse
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G A Stapleton
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M C Phelan
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S Hu
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J Marshall
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H E McDermid
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