Rett networked database: An integrated clinical and genetic network of rett syndrome databases

Human Mutation

Volumn 33, Issue 7, 2012, Pages 1031-1036

  Grillo, Elisa ^a   Villard, Laurent ^b,c   Clarke, Angus ^d   Ben Zeev, Bruria ^e   Pineda, Mercedes ^f   Bahi Buisson, Nadia ^g,h   Hryniewiecka Jaworska, Anna ^d   Bienvenu, Thierry ^h,i   Armstrong, Judith ^f   Martinez, Ana Roche ^f   Mari, Francesca ^a,j   Veneselli, Edvige ^k   Russo, Silvia ^l   Vignoli, Aglaia ^m   Pini, Giorgio ⁿ   Djuric, Milena ^o   Bisgaard, Anne Marie ^p   Mejaški Bošnjak, Vlatka ^q   Polgár, Noémi ^r   Cogliati, Francesca ^l   Ravn, Kirstine ^p   Pintaudi, Maria ^k   Melegh, Béla ^r   Craiu, Dana ^s   Djukic, Aleksandra ^t   Renieri, Alessandra ^a,j   more..

^a UNIVERSITY OF SIENA   (Italy)

^b INSERM   (France)

^c AIX MARSEILLE UNIVERSITY   (France)

^d CARDIFF UNIVERSITY   (United Kingdom)

^e SHEBA MEDICAL CENTER   (Israel)

^f HOSPITAL SANT JOAN DE DÉU   (Spain)

^g HÔPITAL NECKER ENFANTS MALADES   (France)

^h INSTITUT COCHIN   (France)

ⁱ CNRS ^*  (France)

^j UNIVERSITY HOSPITAL OF SIENA   (Italy)

^k UNIVERSITY OF GENOA   (Italy)

^l ISTITUTO AUXOLOGICO ITALIANO   (Italy)

^m SAN PAOLO HOSPITAL   (Italy)

ⁿ Tuscany Rett Centre Versilia Hospital   (Italy)

^o UNIVERSITY OF BELGRADE   (Serbia)

^p JOHN F KENNEDY INSTITUTE   (Denmark)

^q Croatia   (Croatia)

^r UNIVERSITY OF PÉCS   (Hungary)

^s CAROL DAVILA UNIVERSITY OF MEDICINE AND PHARMACY   (Romania)

^t ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

more..

Author keywords

CDKL5; FOXG1; MECP2; Rett Networked Database; Rett syndrome

Indexed keywords

CDKL5 PROTEIN; FOXG1 PROTEIN; METHYL CPG BINDING PROTEIN 2; PHOSPHOTRANSFERASE; UNCLASSIFIED DRUG;

ACCURACY; ARTICLE; CLINICAL STUDY; GENE MUTATION; GENETIC DATABASE; GENETIC VARIABILITY; GENOTYPE PHENOTYPE CORRELATION; INFORMATION PROCESSING; INTERNET; ONLINE SYSTEM; PATIENT INFORMATION; PRIORITY JOURNAL; RETT NETWORKED DATABASE; RETT SYNDROME; STANDARD;

DATABASES, GENETIC; HUMANS; METHYL-CPG-BINDING PROTEIN 2; MUTATION; RETT SYNDROME;

EID: 84861871117     PISSN: 10597794     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.22072     Document Type: Article

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