Add to ORKGLeber hereditary optic neuropathy (LHON) is a mitochondrial genetic disease characterized by bilateral, painless, subacute visual failure that develops during young adult life
Leber hereditary optic neuropathy (LHON) is due primarily to one of three common point mutations of ...
Leber hereditary neuropathy is a maternally inherited mitochondrial disease wich diagnosis is confir...
Leber hereditary optic neuropathy (LHON) is due primarily to one of three common point mutations of ...
Leber's hereditary optic neuropathy (LHON) is an inherited mitochondrial disease that usually le...
AbstractLeber’s hereditary optic neuropathy (LHON) has traditionally been considered a disease causi...
AbstractAt least five mtDNA point mutations appear sufficient in themselves to cause Leber's heredit...
Leber Hereditary Optic Neuropathy (LHON) is one of the most common mitochondrial diseases that can c...
Four new missense mutations have been identified through restriction analysis and sequencing of the ...
Leber's hereditary optic neuropathy (LHON) is a maternally inherited disorder that causes severe los...
is a typical mitochondrial genetic disease that leads to acute or sub-acute visual loss mainly in yo...
Leber hereditary optic neuropathy (LHON) is due primarily to one of three common point mutations of ...
Leber's hereditary optic neuropathy (LHON) is a maternally inherited blinding disorder, which in ove...
Leber's hereditary optic neuropathy (LHON) is a maternally inherited disease associated with mitocho...
Background: Leber’s hereditary optic neuropathy (LHON) is a maternally inherited blinding disorder, ...
Background: Mitochondrial DNA (mtDNA) mutations are known to cause Leber Hereditary Optic Neuropathy...
Leber hereditary optic neuropathy (LHON) is due primarily to one of three common point mutations of ...
Leber hereditary neuropathy is a maternally inherited mitochondrial disease wich diagnosis is confir...
Leber hereditary optic neuropathy (LHON) is due primarily to one of three common point mutations of ...
Leber's hereditary optic neuropathy (LHON) is an inherited mitochondrial disease that usually le...
AbstractLeber’s hereditary optic neuropathy (LHON) has traditionally been considered a disease causi...
AbstractAt least five mtDNA point mutations appear sufficient in themselves to cause Leber's heredit...
Leber Hereditary Optic Neuropathy (LHON) is one of the most common mitochondrial diseases that can c...
Four new missense mutations have been identified through restriction analysis and sequencing of the ...
Leber's hereditary optic neuropathy (LHON) is a maternally inherited disorder that causes severe los...
is a typical mitochondrial genetic disease that leads to acute or sub-acute visual loss mainly in yo...
Leber hereditary optic neuropathy (LHON) is due primarily to one of three common point mutations of ...
Leber's hereditary optic neuropathy (LHON) is a maternally inherited blinding disorder, which in ove...
Leber's hereditary optic neuropathy (LHON) is a maternally inherited disease associated with mitocho...
Background: Leber’s hereditary optic neuropathy (LHON) is a maternally inherited blinding disorder, ...
Background: Mitochondrial DNA (mtDNA) mutations are known to cause Leber Hereditary Optic Neuropathy...
Leber hereditary optic neuropathy (LHON) is due primarily to one of three common point mutations of ...
Leber hereditary neuropathy is a maternally inherited mitochondrial disease wich diagnosis is confir...
Leber hereditary optic neuropathy (LHON) is due primarily to one of three common point mutations of ...