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Pediatric Neurology

Volumn 46, Issue 2, 2012, Pages 127-131

TUBA1A mutation-associated lissencephaly: Case report and review of the literature

(4) Sohal, Aman P S a Montgomery, Tara b Mitra, Dipayan c Ramesh, Venkateswaran a

a Newcastle Upon Tyne Hospitals NHS Foundation Trust (United Kingdom)

b INSTITUTE OF HUMAN GENETICS (United Kingdom)

c NEWCASTLE UPON TYNE HOSPITALS NHS FOUNDATION TRUST (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA TUBULIN; TUBULIN ALPHA 1A; UNCLASSIFIED DRUG;

AGYRIA; ARTICLE; CASE REPORT; CHILD; CLINICAL FEATURE; FEEDING DISORDER; FEMALE; FOLLOW UP; GENE MUTATION; GENETIC ASSOCIATION; GENETIC SCREENING; HUMAN; MEDICAL LITERATURE; PRESCHOOL CHILD; PRIORITY JOURNAL; STRIDOR;

BRAIN; CELL MOVEMENT; EPILEPSY; FEMALE; HUMANS; INFANT; LISSENCEPHALY; PHENOTYPE; TUBULIN;

EID: 84856080222 PISSN: 08878994 EISSN: 18735150 Source Type: Journal
DOI: 10.1016/j.pediatrneurol.2011.11.017 Document Type: Article

Times cited : (38)

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