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Showing results (71-80 of 74) with videos related to

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Journal of the Neurological Sciences|June 15, 2020
Clinical, imaging, morphologic, and molecular features of X-linked VMA21-related myopathy in two unrelated Brazilian familiesAna Cotta, Elmano Carvalho, Antonio Lopes da-Cunha-Junior, et al.
Metallomics : Integrated Biometal Science|June 14, 2016
Characterizing the molecular phenotype of an Atp7a(T985I) conditional knock in mouse model for X-linked distal hereditary motor neuropathy (dHMNX)Gonzalo Perez-Siles, Adrienne Grant, Melina Ellis, et al.
JIMD Reports|July 21, 2020
Early-onset coenzyme Q10 deficiency associated with ataxia and respiratory chain dysfunction due to novel pathogenic <i>COQ8A</i> variants, including a large intragenic deletionAna Cotta, Charlotte L Alston, Sidney Baptista-Junior, et al.
American Journal of Human Genetics|February 23, 2010
Missense mutations in the copper transporter gene ATP7A cause X-linked distal hereditary motor neuropathyMarina L Kennerson, Garth A Nicholson, Stephen G Kaler, et al.
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Showing results (71-80 of 74) with videos related to

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Pageof 8
You have reached the last page of results.This site can display upto 74 results.
Journal of the Neurological Sciences|June 15, 2020
Clinical, imaging, morphologic, and molecular features of X-linked VMA21-related myopathy in two unrelated Brazilian familiesAna Cotta, Elmano Carvalho, Antonio Lopes da-Cunha-Junior, et al.
Metallomics : Integrated Biometal Science|June 14, 2016
Characterizing the molecular phenotype of an Atp7a(T985I) conditional knock in mouse model for X-linked distal hereditary motor neuropathy (dHMNX)Gonzalo Perez-Siles, Adrienne Grant, Melina Ellis, et al.
JIMD Reports|July 21, 2020
Early-onset coenzyme Q10 deficiency associated with ataxia and respiratory chain dysfunction due to novel pathogenic <i>COQ8A</i> variants, including a large intragenic deletionAna Cotta, Charlotte L Alston, Sidney Baptista-Junior, et al.
American Journal of Human Genetics|February 23, 2010
Missense mutations in the copper transporter gene ATP7A cause X-linked distal hereditary motor neuropathyMarina L Kennerson, Garth A Nicholson, Stephen G Kaler, et al.
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