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Exome sequencing in syndromic brain malformations identifies novel mutations in ACTB, and SLC9A6, and suggests BAZ1A as a new candidate gene

Document Type

Article

Author

Weitensteiner, V.; Zhang, R.; Gehlen, J.; Ralser, D.J.; Hilger, A.C.; Schumacher, J.; Reutter, H.; Bungenberg, J.; Becker, A.; Marks, M.; Herrmann, B.G.; Sharma, A.; Gembruch, U.; Merz, W.M.; Altmüller, J.; Thiele, H.; Odermatt, B.; Ludwig, M.

Source

In: Birth Defects Research. (Birth Defects Research, 17 April 2018, 110(7):587-597)

Subject

Language

English

ISSN

24721727

Online Access

Full Text (Wiley Journals) Full Text (Wiley-DB) Web of Science JCR 저널정보 Scopus Find it@PNU

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