Hypokalemic periodic paralysis mutations: confirmation of mutation and analysis of founder effect

scientific article published on 01 January 1996

Hypokalemic periodic paralysis mutations: confirmation of mutation and analysis of founder effect is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1016/0960-8966(95)00018-6
P698PubMed publication ID8845715

P50authorJames F. GusellaQ1602688
P2093author name stringBrown RH Jr
Esteban J
McKenna-Yasek D
Grosson CL
P433issue1
P921main subjectfounder effectQ504568
hypokalemic periodic paralysisQ622828
P304page(s)27-31
P577publication date1996-01-01
P1433published inNeuromuscular DisordersQ1981326
P1476titleHypokalemic periodic paralysis mutations: confirmation of mutation and analysis of founder effect
P478volume6

Reverse relations

cites work (P2860)
Q33599318A Korean family of hypokalemic periodic paralysis with mutation in a voltage-gated calcium channel (R1239G)
Q27675997Aromatic Sulfonyl Fluorides Covalently Kinetically Stabilize Transthyretin to Prevent Amyloidogenesis while Affording a Fluorescent Conjugate
Q30779129Bisaryloxime ethers as potent inhibitors of transthyretin amyloid fibril formation
Q57665572Comparative calorimetric study of non-amyloidogenic and amyloidogenic variants of the homotetrameric protein transthyretin
Q30603364Etiology of hypokalemic paralysis in Korea: data from a single center
Q36774708Hypokalemic periodic paralysis: a model for a clinical and research approach to a rare disorder
Q41510537Hypokalemic periodic paralysis: an autosomal dominant muscle disorder caused by mutations in a voltage-gated calcium channel.
Q35054061Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family
Q82029865Periodic paralysis
Q74763599Severe hypokalemia as a cause of acute transient paraplegia following electrical shock
Q29398134The Genotype and Clinical Phenotype of Korean Patients with Familial Hypokalemic Periodic Paralysis
Q57665578The amyloidogenic potential of transthyretin variants correlates with their tendency to aggregate in solution
Q34438326The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein
Q33510262The role of CACNA1S in predisposition to malignant hyperthermia

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