Novel pathogenic ACAN variants in non-syndromic short stature patients.

Clinica Chimica Acta(2017)

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摘要
•First ACAN mutation screening among short stature patients was conducted.•A high prevalence of ACAN mutation was reported.•ACAN mutation is a relative common cause of familial severe short stature.•The spectrums of clinical phenotype and ACAN mutation were further extended.
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关键词
SEDK,OD,SEMD,ISS,rhGH,OA,pLI,CLD,ExAC
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