An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness
TM Strom, G Nyakatura, E Apfelstedt-Sylla… - Nature …, 1998 - nature.com
The locus for the incomplete form of X-linked congenital stationary night blindness (CSNB2)
maps to a 1.1-Mb region in Xp11. 23 between markers DXS722 and DXS255. We identified …
maps to a 1.1-Mb region in Xp11. 23 between markers DXS722 and DXS255. We identified …
[PDF][PDF] An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness
TM Strom, G Nyakatura, E Apfelstedt-Sylla… - nature …, 1998 - academia.edu
The locus for the incomplete form of X-linked congenital stationary night blindness (CSNB2)
maps to a 1.1-Mb region in Xp11. 23 betw een markers DXS722 and DXS255. We identified …
maps to a 1.1-Mb region in Xp11. 23 betw een markers DXS722 and DXS255. We identified …
[PDF][PDF] An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness
TM Strom, G Nyakatura, E Apfelstedt-Sylla… - nature …, 1998 - researchgate.net
The locus for the incomplete form of X-linked congenital stationary night blindness (CSNB2)
maps to a 1.1-Mb region in Xp11. 23 between markers DXS722 and DXS255. We identified …
maps to a 1.1-Mb region in Xp11. 23 between markers DXS722 and DXS255. We identified …
[引用][C] An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness
TM STROM, G NYAKATURA, C SAUER… - Nature …, 1998 - pascal-francis.inist.fr
An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night
blindness CNRS Inist Pascal-Francis CNRS Pascal and Francis Bibliographic Databases …
blindness CNRS Inist Pascal-Francis CNRS Pascal and Francis Bibliographic Databases …
An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness
TM Strom, G Nyakatura, E Apfelstedt-Sylla… - Nature …, 1998 - epub.uni-regensburg.de
The locus for the incomplete form of X-linked congenital stationary night blindness (CSNB2)
maps to a 1.1-Mb region in Xp11. 23 between markers DXS722 and DXS255. We identified …
maps to a 1.1-Mb region in Xp11. 23 between markers DXS722 and DXS255. We identified …
[PDF][PDF] An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness
TM Strom, G Nyakatura, E Apfelstedt-Sylla… - nature …, 1998 - genome.leibniz-fli.de
The locus for the incomplete form of X-linked congenital stationary night blindness (CSNB2)
maps to a 1.1-Mb region in Xp11. 23 between markers DXS722 and DXS255. We identified …
maps to a 1.1-Mb region in Xp11. 23 between markers DXS722 and DXS255. We identified …
An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness.
TM Strom, G Nyakatura, E Apfelstedt-Sylla… - Nature …, 1998 - europepmc.org
The locus for the incomplete form of X-linked congenital stationary night blindness (CSNB2)
maps to a 1.1-Mb region in Xp11. 23 between markers DXS722 and DXS255. We identified …
maps to a 1.1-Mb region in Xp11. 23 between markers DXS722 and DXS255. We identified …
An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness
TM Strom, G Nyakatura, E Apfelstedt-Sylla… - Nature …, 1998 - pubmed.ncbi.nlm.nih.gov
The locus for the incomplete form of X-linked congenital stationary night blindness (CSNB2)
maps to a 1.1-Mb region in Xp11. 23 between markers DXS722 and DXS255. We identified …
maps to a 1.1-Mb region in Xp11. 23 between markers DXS722 and DXS255. We identified …
An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness.
TM Strom, G Nyakatura, E Apfelstedt-Sylla… - Nature …, 1998 - search.ebscohost.com
The locus for the incomplete form of X-linked congenital stationary night blindness (CSNB2)
maps to a 1.1-Mb region in Xp11. 23 between markers DXS722 and DXS255. We identified …
maps to a 1.1-Mb region in Xp11. 23 between markers DXS722 and DXS255. We identified …
[PDF][PDF] An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness
TM Strom, G Nyakatura, E Apfelstedt-Sylla… - nature …, 1998 - genome.imb-jena.de
The locus for the incomplete form of X-linked congenital stationary night blindness (CSNB2)
maps to a 1.1-Mb region in Xp11. 23 between markers DXS722 and DXS255. We identified …
maps to a 1.1-Mb region in Xp11. 23 between markers DXS722 and DXS255. We identified …