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[ON THE GENETICS OF MYOTONIAS (A PRELIMINARY SURVEY)]

Overview
Journal Internist (Berl)
Specialty General Medicine
Date 1963 Sep 1
PMID 14092155
Citations 9
Authors
P E BECKER
Affiliations
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Citing Articles

Molecular Characterization in 19 South-Italian Patients With Dominant and Recessive Type of Myotonia Congenita.

Orsini C, Petillo R, DAmbrosio P, Ergoli M, Picillo E, Scutifero M Front Neurol. 2020; 11:63.

PMID: 32117024 PMC: 7016095. DOI: 10.3389/fneur.2020.00063.

[CHROMOSOME STUDIES IN MYOTONIA].

Eberle P, BECKER P Humangenetik. 1964; 1:92-7.

PMID: 14338384 DOI: 10.1007/BF00289367.

[MYOTONIA AND KLINEFELTER SYNDROME].

BECKER P, Eberle P Humangenetik. 1964; 1:83-91.

PMID: 14338383 DOI: 10.1007/BF00289366.

[Genetic contribution to the problem of the late form of Pelizaeus-Merzbacher disease].

PEIFFER J Humangenetik. 1964; 1(2):107-22.

PMID: 5869474 DOI: 10.1007/BF00389627.

[Metabolic studies and exchange of 42 K in a case of periodic hyperkalemic paralysis with myotonic symptoms].

ULBRICHT W, SCHWARTZKOPFF W Dtsch Z Nervenheilkd. 1969; 195(2):103-14.

PMID: 5805676