Citations for
1FKRP, FKTN, ITGA7, LAMA2, MDC1A, MDC1B, POMGNT1, POMT1, RSMD1, SEPN1, WLKWS1, WLKWS4
Case 35-2006 -- A Newborn Boy with Hypotonia.
Brown RH Jr, Grant PE, Pierson CR.
N Engl J Med 355(20):2132-2142. No abstract available. 2006
2ITGA7
The LIM-only proteins FHL2 and FHL3 interact with alpha- and beta-subunits of the muscle alpha7beta1 integrin receptor.
Samson T, Smyth N, Janetzky S, Wendler O, Muller JM, Schule R, von der Mark H, von der Mark K, Wixler V.
J Biol Chem 279(27):28641-52. Epub 2004 Apr 26. 2004
3ITGA7
Structure, genetic localization, and identification of the cardiac and skeletal muscle transcripts of the human integrin alpha7 gene (ITGA7).
Vignier N, et al.
Biochem Biophys Res Commun 260(2):357-64 1999
4ITGA7
Mutations in the integrin alpha7 gene cause congenital myopathy.
Hayashi YK, et al.
Nat Genet 19 : 94-97. 1998
5ITGA7
Absence of integrin alpha 7 causes a novel form of muscular dystrophy.
Mayer U, Saher G, Fassler R, Bornemann A, Echtermeyer F, von der Mark H, Miosge N, Poschl E, von der Mark K.
Nat Genet 17(3):318-23. 1997
6ITGA7, ITGB8
Localization of the alpha7 integrin gene (ITGA7) on human chromosome 12q13 : clustering of integrin and hox genes implies parallel evolution of these gene families.
Wang W, et al.
Genomics 26 : 563-570. 1995