Article
Occipital cortex dysgenesis with white matter changes due to mutations in Laminin a2.
The Turkish journal of pediatrics - 1 Jan 2017
Yiş Uluç, Dixit Vishal, Işıkay Sedat, Karakaya Mert, Baydan Figen, Diniz Gülden, Polat İpek, Hız-Kurul Semra, Çırak Sebahattin
Abstract excerpt
Yiş U, Dixit V, Işıkay S, Karakaya M, Baydan F, Diniz G, Polat İ, Hız-Kurul S, Çırak S. Occipital cortex dysgenesis with white matter changes due to mutations in Laminin a2. Turk J Pediatr 2017; 59: 338-341. Laminin α2 related congenital muscular dystrophy is one of the most common congenital muscular dystrophies of childhood with or without clinical evidence of central nervous system involvement. It may be...
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