FSCN1 as a Candidate Gene for Syndromic Intellectual Disability? Evidence From a Recurrent Variant in an Iranian Cohort
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DOI: 10.1111/cge.70051
文献链接: https://onlinelibrary.wiley.com/doi/10.1111/cge.70051
其他信息:
出版社: Wiley
作者: Hossein Najmabadi; Tara Akhtarkhavari; Ebrahim Shokouhian; Sanaz Arzhangi; Kimia Kahrizi

