Heterozygous 'null allele' mutation in the human peripherin/RDS gene.
Meins, M
Heterozygous 'null allele' mutation in the human peripherin/RDS gene. [electronic resource] - Human molecular genetics Dec 1993 - 2181-2 p. digital
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
0964-6906
10.1093/hmg/2.12.2181 doi
Alleles
Animals
Arginine
Base Sequence
Exons
Genetic Carrier Screening
Humans
Intermediate Filament Proteins--genetics
Male
Membrane Glycoproteins
Mice
Middle Aged
Mutation
Nerve Tissue Proteins
Neuropeptides--genetics
Peripherins
Polymerase Chain Reaction
Retinal Degeneration--genetics
Heterozygous 'null allele' mutation in the human peripherin/RDS gene. [electronic resource] - Human molecular genetics Dec 1993 - 2181-2 p. digital
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
0964-6906
10.1093/hmg/2.12.2181 doi
Alleles
Animals
Arginine
Base Sequence
Exons
Genetic Carrier Screening
Humans
Intermediate Filament Proteins--genetics
Male
Membrane Glycoproteins
Mice
Middle Aged
Mutation
Nerve Tissue Proteins
Neuropeptides--genetics
Peripherins
Polymerase Chain Reaction
Retinal Degeneration--genetics