Mutation of FLNA attenuating the migration of abdominal muscles contributed to Melnick–Needles syndrome (MNS) in a family with recurrent miscarriage

Abstract Background Filamin A, encoded by the X‐linked gene FLNA, links the cell membrane with the cytoskeleton and acts as a regulator of the actin cytoskeleton. Mutations in FLNA cause a large spectrum of congenital malformations during embryonic development, including Melnick–Needles syndrome (MN...

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Autors principals:	Xin Luo, Zailin Yang, Jing Zeng, Jing Chen, Ningxuan Chen, Xiaoyan Jiang, Qinlv Wei, Ping Yi, Jing Xu
Format:	Artigo
Idioma:	Inglês
Publicat:	Wiley 2023-05-01
Col·lecció:	Molecular Genetics & Genomic Medicine
Matèries:	FLNA Melnick–Needles syndrome midline structure dysplasia recurrent miscarriage
Accés en línia:	https://doi.org/10.1002/mgg3.2145
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