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Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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M Papazian

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Neurology|November 28, 2001

Loss-of-function EA2 mutations are associated with impaired neuromuscular transmissionJ Jen, J Wan, M Graves, et al.

Plos One|April 12, 2011

Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13)Karla P Figueroa, Michael F Waters, Vartan Garibyan, et al.

Human Mutation|December 3, 2009

KCNC3: phenotype, mutations, channel biophysics-a study of 260 familial ataxia patientsKarla P Figueroa, Natali A Minassian, Giovanni Stevanin, et al.

Cellular and Molecular Life Sciences : CMLS|April 10, 2015

Spinocerebellar ataxia type 19/22 mutations alter heterocomplex Kv4.3 channel function and gating in a dominant mannerAnna Duarri, Meng-Chin A Lin, Michiel R Fokkens, et al.

American Journal of Human Genetics|October 6, 2000

Identification of MEFV-independent modifying genetic factors for familial Mediterranean feverC Cazeneuve, H Ajrapetyan, S Papin, et al.

Nature Genetics|February 28, 2006

Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypesMichael F Waters, Natali A Minassian, Giovanni Stevanin, et al.

Pageof 7

Search research articles

Showing results (61-70 of 66) with videos related to

Sort By:

Pageof 7

You have reached the last page of results.This site can display upto 66 results.

Neurology|November 28, 2001

Loss-of-function EA2 mutations are associated with impaired neuromuscular transmissionJ Jen, J Wan, M Graves, et al.

Plos One|April 12, 2011

Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13)Karla P Figueroa, Michael F Waters, Vartan Garibyan, et al.

Human Mutation|December 3, 2009

KCNC3: phenotype, mutations, channel biophysics-a study of 260 familial ataxia patientsKarla P Figueroa, Natali A Minassian, Giovanni Stevanin, et al.

Cellular and Molecular Life Sciences : CMLS|April 10, 2015

Spinocerebellar ataxia type 19/22 mutations alter heterocomplex Kv4.3 channel function and gating in a dominant mannerAnna Duarri, Meng-Chin A Lin, Michiel R Fokkens, et al.

American Journal of Human Genetics|October 6, 2000

Identification of MEFV-independent modifying genetic factors for familial Mediterranean feverC Cazeneuve, H Ajrapetyan, S Papin, et al.

Nature Genetics|February 28, 2006

Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypesMichael F Waters, Natali A Minassian, Giovanni Stevanin, et al.

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