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A prenatal case of lissencephaly with cerebellar hypoplasia: New mutation in RELN gene

Document Type

Article

Author

Balza, C.; Garofalo, G.; Cassart, M.; Ben Abbou, W.; Cos, T.; Kang, X.; Désir, J.; Keymolen, K.; Van Berkel, K.; Soblet, J.; Vilain, C.

Source

In: Clinical Case Reports. (Clinical Case Reports, December 2021, 9(12))

Subject

Language

English

ISSN

20500904

Online Access

Full Text (ProQuest Central) Full Text (Gale Academic Onefile) Open Access (Wiley) Web of Science JCR 저널정보 Scopus Find it@PNU

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