Isolation and Characterization of a Calcium Channel Gene, Cacna1f, the Murine Orthologue of the Gene for Incomplete X-Linked Congenital Stationary Night Blindness
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference13 articles.
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2. High-resolution comparative mapping of the proximal region of the mouse X chromosome;Blair;Genomics,1995
3. Essential Ca2+-binding motif for Ca2+-sensitive inactivation of L-type Ca2+ channels;de Leon;Science,1995
4. Sequence-based exon prediction around the synaptophysin locus reveals a gene-rich area containing novel genes in human proximal Xp;Fisher;Genomics,1997
5. Developmental expression patterns of mouse sFRP genes encoding members of the secreted frizzled related protein family;Leimeister;Mech. Dev.,1998
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