Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17

Author:

Koch ManuelaC.,Ricker Kenneth,Otto Michael,Grimm Tiemo,Bender Klaus,Zoll Barbara,Harper PeterS.,Lehmann-Horn Frank,R�del Reinhardt,Hoffman EricP.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Reference27 articles.

1. Becker PE (1970) Paramyotonia congenita (Eulenburg). (Fortschritte der allgemeinen und klinischen Humangenetik). Thieme, Stuttgart

2. Becker PE (1977) Myotonia congenita and syndromes associated with myotonia. (Topics in human genetics) Thieme, Stuttgart

3. Chakravarti A, Phillipps JA, Mellitis KH, Buetow KH, Seeburg PH (1984) Patterns of polymorphisms and linkage disequilibrium suggest independent origins of the human growth hormone gene cluster. Proc Natl Acad Sci USA 81:6085?6089

4. De Silva SM, Kuncl RW, Griffin JW, Cornblath DR, Chavoustie S (1990) Paramyotonia congenita or hyperkalemic periodic paralysis? Clinical and electrophysiological features of each entity in one family. Muscle Nerve 13:21?26

5. Engel AG (1986) Periodic paralysis. In: Engel AG, Banker BO (eds) Myology. McGraw-Hill, New York, pp 1843?1870

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