A TNNI2 mutation in a family with distal arthrogryposis type 2B
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference6 articles.
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3. A variant of Freeman-Sheldon syndrome maps to 11p15.5-pter;Krakowiak;Am. J. Hum. Genet.,1997
4. Mapping a gene (MRXS9) for X-linked mental retardation, microcephaly, and variable short stature to Xq12-q21.31;Shrimpton;Am. J. Med. Genet.,1999
5. Mutations in genes encoding fast-twitch contractile proteins cause distal arthrogryposis syndromes;Sung;Am. J. Hum. Genet.,2003
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