The protein kinase N (PKN) gene PRKCL1/Prkcl1 maps to human chromosome 19p12-p13.1 and mouse chromosome 8 with close linkage to the myodystrophy (myd) mutation.
Bartsch, J W
The protein kinase N (PKN) gene PRKCL1/Prkcl1 maps to human chromosome 19p12-p13.1 and mouse chromosome 8 with close linkage to the myodystrophy (myd) mutation. [electronic resource] - Genomics Apr 1998 - 129-32 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0888-7543
10.1006/geno.1997.5208 doi
Animals
Chromosome Mapping
Chromosomes, Human, Pair 19
Female
Genetic Linkage
Humans
In Situ Hybridization, Fluorescence
Male
Mice
Mice, Inbred C57BL
Muscular Dystrophy, Animal--genetics
Mutation
Protein Kinase C--genetics
The protein kinase N (PKN) gene PRKCL1/Prkcl1 maps to human chromosome 19p12-p13.1 and mouse chromosome 8 with close linkage to the myodystrophy (myd) mutation. [electronic resource] - Genomics Apr 1998 - 129-32 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0888-7543
10.1006/geno.1997.5208 doi
Animals
Chromosome Mapping
Chromosomes, Human, Pair 19
Female
Genetic Linkage
Humans
In Situ Hybridization, Fluorescence
Male
Mice
Mice, Inbred C57BL
Muscular Dystrophy, Animal--genetics
Mutation
Protein Kinase C--genetics