A "dystrophic" variant of autosomal recessive myotonia congenita caused by novel mutations in the CLCN1 gene (Q73289009)
scientific article published on 01 December 2000
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Current Data About A "dystrophic" variant of autosomal recessive myotonia congenita caused by novel mutations in the CLCN1 gene
(P31) (Q13442814)
(P248)
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(P813) Saturday, November 2, 2019

(P50) (Q73274432)
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(P304) 1697-1703
(P248)
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(P813) Saturday, November 2, 2019

(P407) (Q1860)

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(P813) Saturday, November 2, 2019

(P478) 55
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(P813) Saturday, November 2, 2019

(P577) Friday, December 1, 2000
(P248)
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(P813) Saturday, November 2, 2019

(P921) (Q587420)
(P887)

(P1433) (Q1161692)
(P248)
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(P1476) "A "dystrophic" variant of autosomal recessive myotonia congenita caused by novel mutations in the CLCN1 gene" (language: en)
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(P854) https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11113225%20AND%20SRC:MED&resulttype=core&format=json
(P813) Saturday, November 2, 2019

(P2093) S Nagamitsu
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(P813) Saturday, November 2, 2019

T Matsuura
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(P813) Saturday, November 2, 2019

M Khajavi
(P1545) 3
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R Armstrong
(P1545) 4
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Y Harati
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(P813) Saturday, November 2, 2019

T Ashizawa
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(P854) https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11113225%20AND%20SRC:MED&resulttype=core&format=json
(P813) Saturday, November 2, 2019

other details
description scientific article published on 01 December 2000

External Links
(P356) 10.1212/WNL.55.11.1697
(P698) 11113225