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A Novel Splicing Mutation c.335-1 G > A in the Cardiac Transcription Factor NKX2-5 Leads to Familial Atrial Septal Defect Through miR-19 and PYK2.
Stem Cell Rev Rep. 2022 Dec;18(8):2646-2661. doi: 10.1007/s12015-022-10400-5. Epub 2022 Jul 2.
Stem Cell Rev Rep. 2022.
PMID: 35778654
First report of a novel LMNA mutation in a Chinese family with limb-girdle muscular dystrophy.
Hong G, Dan Z, Limeng D, Luxiang C, Bai Y.
Hong G, et al. Among authors: limeng d.
J Genet. 2014 Dec;93(3):843-7. doi: 10.1007/s12041-014-0445-1.
J Genet. 2014.
PMID: 25572245
Free article.
No abstract available.
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