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Mus musculus nuclear factor I/B (Nfib), transcript variant 2, mRNA
Mus musculus nuclear factor I/B (Nfib), transcript variant 2, mRNA
gi|2719984711|ref|NM_001113210.3|
Nucleotide
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Hepatolenticular Degeneration
Hepatolenticular Degeneration
A rare autosomal recessive disease characterized by the deposition of copper in the BRAIN; LIVER; CORNEA; and other organs. It is caused by defects in the ATP7B gene encoding ...<br/>Year introduced: 1964(1963)
MeSH
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Homocystinuria
Homocystinuria
Autosomal recessive inborn error of methionine metabolism usually caused by a deficiency of CYSTATHIONINE BETA-SYNTHASE and associated with elevations of homocysteine in plasm...<br/>Year introduced: 1969(1967)
MeSH
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