Netrin G1 Mutations Are an Uncommon Cause of Atypical Rett Syndrome With or Without Epilepsy

Pediatric Neurology

Volumn 37, Issue 4, 2007, Pages 270-274

  Nectoux, Juliette ^a,b   Girard, Benoit ^a   Bahi Buisson, Nadia ^c   Prieur, Fabienne ^d   Afenjar, Alexandra ^e   Rosas Vargas, Haydee ^b   Chelly, Jamel ^a,b   Bienvenu, Thierry ^a,b  

^a Hôpital Cochin ^*  (France)

^b CNRS   (France)

^c HÔPITAL NECKER ENFANTS MALADES   (France)

^d HÔPITAL NORD   (France)

^e ARMAND TROUSSEAU HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CPG BINDING PROTEIN 2; GENE PRODUCT; LEUCINE; UNCLASSIFIED DRUG; VALINE;

ADOLESCENT; AMINO ACID SUBSTITUTION; ARTICLE; CHILD; CLINICAL FEATURE; CONTROLLED STUDY; EPILEPSY; FEMALE; GENE; GENE FREQUENCY; GENE IDENTIFICATION; GENE MUTATION; GENE TRANSLOCATION; GENETIC VARIABILITY; HUMAN; MAJOR CLINICAL STUDY; NETRIN G1 GENE; PHENOTYPE; PRIORITY JOURNAL; RETT SYNDROME;

ADOLESCENT; ADULT; AMINO ACID SUBSTITUTION; BASE SEQUENCE; BRAIN DISEASES; CHILD; CHILD, PRESCHOOL; EPILEPSY; FEMALE; GLYCOPROTEINS; HUMANS; LEUCINE; MUTATION; NERVE TISSUE PROTEINS; PHENOTYPE; RETT SYNDROME; VALINE; VARIATION (GENETICS);

EID: 34548832777     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pediatrneurol.2007.06.002     Document Type: Article

References (11)

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