The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein. Read more about The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein.
Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21. Read more about Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21.
Mapping of a major genetic modifier of embryonic lethality in TGF beta 1 knockout mice. Read more about Mapping of a major genetic modifier of embryonic lethality in TGF beta 1 knockout mice.
P1148A in fibrillin-1 is not a mutation anymore. Read more about P1148A in fibrillin-1 is not a mutation anymore.
Leptin activation of Stat3 in the hypothalamus of wild-type and ob/ob mice but not db/db mice. Read more about Leptin activation of Stat3 in the hypothalamus of wild-type and ob/ob mice but not db/db mice.
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Read more about A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis.
A full genome search in multiple sclerosis. Read more about A full genome search in multiple sclerosis.
Spontaneous in vivo reversion to normal of an inherited mutation in a patient with adenosine deaminase deficiency. Read more about Spontaneous in vivo reversion to normal of an inherited mutation in a patient with adenosine deaminase deficiency.
A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2. Read more about A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2.
