FKRP (826C>A) frequently causes limb-girdle muscular dystrophy in German patients.

Journal of medical genetics

Volumn 41, Issue 4, 2004, Pages

  Walter, M C ^a   Petersen, J A ^a   Stucka, R ^a   Fischer, D ^a   Schroder R ^a   Vorgerd, M ^a   Schroers, A ^a   Schreiber, H ^a   Hanemann, C O ^a   Knirsch, U ^a   Rosenbohm, A ^a   Huebner, A ^a   Barisic, N ^a   Horvath, R ^a   Komoly, S ^a   Reilich, P ^a   Muller Felber W ^a   Pongratz, D ^a   Muller J S ^a   Auerswald, E A ^a   Lochmuller H ^a   more..

^a LUDWIG MAXIMILIANS UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

FKRP PROTEIN, HUMAN; PROTEIN;

ADOLESCENT; ADULT; AMINO ACID SEQUENCE; ARTICLE; CHILD; FEMALE; GENE FREQUENCY; GENETIC POLYMORPHISM; GENETICS; GERMANY; HUMAN; IMMUNOHISTOCHEMISTRY; MALE; MIDDLE AGED; MISSENSE MUTATION; MOLECULAR GENETICS; MUSCULAR DYSTROPHY; POINT MUTATION; SEQUENCE ALIGNMENT;

ADOLESCENT; ADULT; AMINO ACID SEQUENCE; CHILD; FEMALE; GENE FREQUENCY; GERMANY; HUMANS; IMMUNOHISTOCHEMISTRY; MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MUSCULAR DYSTROPHIES; MUTATION, MISSENSE; POINT MUTATION; POLYMORPHISM, GENETIC; PROTEINS; SEQUENCE ALIGNMENT;

EID: 2342590096     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.2003.013953     Document Type: Article

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