Identification of mutations in AP4S1/ SPG52 through next generation sequencing in three families-Reference-Cited by-同舟云学术

Identification of mutations in AP4S1/ SPG52 through next generation sequencing in three families

Author:

Tessa A.¹,Battini R.²,Rubegni A.¹,Storti E.¹,Marini C.³,Galatolo D.¹,Pasquariello R.⁴,Santorelli F. M.¹²

Affiliation:

1. Molecular Medicine and Neurogenetics IRCCS Stella Maris Pisa Italy

2. Child Neurology IRCCS Stella Maris Pisa Italy

3. Pediatric Neurology Unit Children's Hospital ‘A. Meyer’ University of Florence FlorenceItaly

4. Neuroradiology IRCCS Stella Maris Pisa Italy

Funder

Italian Ministry of Health

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

Reference20 articles.

3. A report: the definition and classification of cerebral palsy April 2006;Rosenbaum P;Dev Med Child Neurol Suppl,2007

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