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[HTML][HTML] Hypermanganesemia with dystonia 1

2021 - europepmc.org
Hypermanganesemia with dystonia 1 (HMNDYT1) is characterized by the following: A
movement disorder resulting from manganese accumulation in the basal ganglia. Whole …
被引用次数：4 相关文章

Hypermanganesemia with Dystonia 1

K Tuschl, PT Clayton, SM Gospe Jr… - GeneReviews® …, 1993 - pubmed.ncbi.nlm.nih.gov
Clinical characteristics Hypermanganesemia with dystonia 1 (HMNDYT1) is characterized
by the following: A movement disorder resulting from manganese accumulation in the basal …
[HTML] europepmc.org

[HTML][HTML] Hypermanganesemia with Dystonia 1

K Tuschl, PT Clayton, SM Gospe Jr, PB Mills - 2021 - europepmc.org
Hypermanganesemia with dystonia 1 (HMNDYT1) is characterized by the following: A
movement disorder resulting from manganese accumulation in the basal ganglia. Whole …
[HTML] nih.gov

[HTML][HTML] Hypermanganesemia with Dystonia 1

K Tuschl, PT Clayton, SM Gospe Jr… - GeneReviews®[Internet …, 2021 - ncbi.nlm.nih.gov
Neurologic findings can manifest in childhood (ages 2-15 years) as four-limb dystonia,
leading to a characteristic high-stepping gait (" cock-walk gait"), dysarthria, fine tremor, and …
[HTML] nih.gov

[HTML][HTML] Hypermanganesemia with Dystonia 1

K Tuschl, PT Clayton, SM Gospe Jr… - GeneReviews®[Internet …, 2021 - ncbi.nlm.nih.gov
Neurologic findings can manifest in childhood (ages 2-15 years) as four-limb dystonia,
leading to a characteristic high-stepping gait (" cock-walk gait"), dysarthria, fine tremor, and …