Exome sequencing reveals a novel CWF19L1...

American Journal of Medical Genetics Part A 2016 / 06 Vol. 170; Iss. 6

Exome sequencing reveals a novel CWF19L1 mutation associated with intellectual disability and cerebellar atrophy

Evers, Christina, Kaufmann, Lilian, Seitz, Angelika, Paramasivam, Nagarajan, Granzow, Martin, Karch, Stephanie, Fischer, Christine, Hinderhofer, Katrin, Gdynia, Georg, Elsässer, Michael, Pinkert, Stef
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Volume:
170
Language:
english
Journal:
American Journal of Medical Genetics Part A
DOI:
10.1002/ajmg.a.37632
Date:
June, 2016
File:
PDF, 1.53 MB
english, 2016
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