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12. Identification of a novel CNTNAP1 mutation causing arthrogryposis multiplex congenita with cerebral and cerebellar atrophy. Lakhani S; Doan R; Almureikhi M; Partlow JN; Al Saffar M; Elsaid MF; Alaaraj N; James Barkovich A; Walsh CA; Ben-Omran T Eur J Med Genet; 2017 May; 60(5):245-249. PubMed ID: 28254648 [TBL] [Abstract][Full Text] [Related]