TY  - GEN
AU  - Kark,R A
AU  - Becker,D M
TI  - Multiple genotypes, multiple phenotypes, and partial defects
SN  - 0148-639X
PY  - 1981///0723
KW  - Anemia, Hemolytic, Congenital
KW  - genetics
KW  - Arylsulfatases
KW  - deficiency
KW  - Female
KW  - Genetic Variation
KW  - Genotype
KW  - Glucosephosphate Dehydrogenase Deficiency
KW  - Glycogen Storage Disease Type V
KW  - Humans
KW  - Hyperlipoproteinemia Type II
KW  - Male
KW  - Models, Genetic
KW  - Muscular Atrophy
KW  - Neuromuscular Diseases
KW  - Phenotype
KW  - Porphyrias
KW  - Pyruvate Kinase
KW  - Tay-Sachs Disease
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.; Review
UR  - https://doi.org/10.1002/mus.880040107
ER  -