Mutations in PRRT2 are not a common cause of infantile epileptic encephalopathies. [electronic resource]

By:

Heron, Sarah E

Contributor(s):

Ong, Yeh Sze
Yendle, Simone C
McMahon, Jacinta M
Berkovic, Samuel F
Scheffer, Ingrid E
Dibbens, Leanne M

Producer: 20130625Description: e86-9 p. digitalISSN:

1528-1167

Subject(s):

Age Factors
Cohort Studies
DNA Mutational Analysis
Female
Gene Frequency
Genetic Predisposition to Disease -- genetics
Humans
Infant
Male
Membrane Proteins -- genetics
Mutation -- genetics
Nerve Tissue Proteins -- genetics
Phenotype
Spasms, Infantile -- genetics

Online resources:

Available from publisher's website

In: Epilepsia vol. 54

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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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Mutations in PRRT2 are not a common cause of infantile epileptic encephalopathies.

APA

Heron S. E., Ong Y. S., Yendle S. C., McMahon J. M., Berkovic S. F., Scheffer I. E. & Dibbens L. M. (20130625). Mutations in PRRT2 are not a common cause of infantile epileptic encephalopathies. : Epilepsia.

Chicago

Heron Sarah E, Ong Yeh Sze, Yendle Simone C, McMahon Jacinta M, Berkovic Samuel F, Scheffer Ingrid E and Dibbens Leanne M. 20130625. Mutations in PRRT2 are not a common cause of infantile epileptic encephalopathies. : Epilepsia.

Harvard

Heron S. E., Ong Y. S., Yendle S. C., McMahon J. M., Berkovic S. F., Scheffer I. E. and Dibbens L. M. (20130625). Mutations in PRRT2 are not a common cause of infantile epileptic encephalopathies. : Epilepsia.

MLA

Heron Sarah E, Ong Yeh Sze, Yendle Simone C, McMahon Jacinta M, Berkovic Samuel F, Scheffer Ingrid E and Dibbens Leanne M. Mutations in PRRT2 are not a common cause of infantile epileptic encephalopathies. : Epilepsia. 20130625.

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