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Subject Item

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научни чланак სამეცნიერო სტატია article scientific naučni članak artículo científico publicado en 2007 article scientifique (publié 2007) 2007年論文 บทความทางวิทยาศาสตร์ article científic 2007年论文 artigo científico (publicado na 2007) 2007年论文 2007年論文 videnskabelig artikel (udgivet 2007) mokslinis straipsnis articol științific wetenschappelijk artikel (gepubliceerd in 2007-09) мақолаи илмӣ bilimsel makale 2007年论文 наукова стаття, опублікована у вересні 2007 artikulong pang-agham vitenskapelig artikkel научная статья tieteellinen artikkeli سائنسی مضمون 2007年論文 artigo científico (publicado na 2007) 2007年论文 2007 թվականի սեպտեմբերին հրատարակված գիտական հոդված artykuł naukowy scienca artikolo научни чланак tudományos cikk مقالهٔ علمی 2007년 논문 ২০০৭-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ 2007 nî lūn-bûn vitskapeleg artikkel vetenskaplig artikel 2007年論文 2007 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած scientific article bài báo khoa học 2007年论文 artikull shkencor vedecký článok (publikovaný 2007-09) articolo scientifico научна статия 2007年论文 מאמר מדעי مقالة علمية (نشرت في سبتمبر 2007) wissenschaftlicher Artikel επιστημονικό άρθρο мақолаи илмӣ 2007年の論文 2007年論文 artigo científico teaduslik artikkel artículu científicu espublizáu en 2007 vědecký článek publikovaný v roce 2007

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2007-09-01T00:00:00Z

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Homa Tajsharghi Monica Ohlsson Anders Oldfors Christopher Lindberg

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4007479

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Congenital myopathy with nemaline rods and cap structures caused by a mutation in the beta-tropomyosin gene (TPM2) Congenital myopathy with nemaline rods and cap structures caused by a mutation in the beta-tropomyosin gene (TPM2) Congenital myopathy with nemaline rods and cap structures caused by a mutation in the beta-tropomyosin gene (TPM2)

skos:prefLabel

Congenital myopathy with nemaline rods and cap structures caused by a mutation in the beta-tropomyosin gene (TPM2) Congenital myopathy with nemaline rods and cap structures caused by a mutation in the beta-tropomyosin gene (TPM2) Congenital myopathy with nemaline rods and cap structures caused by a mutation in the beta-tropomyosin gene (TPM2)

schema:name

Congenital myopathy with nemaline rods and cap structures caused by a mutation in the beta-tropomyosin gene (TPM2) Congenital myopathy with nemaline rods and cap structures caused by a mutation in the beta-tropomyosin gene (TPM2) Congenital myopathy with nemaline rods and cap structures caused by a mutation in the beta-tropomyosin gene (TPM2)

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wds:Q28248133-D52B8589-B498-45E4-8B9E-4C9E65732342

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Congenital myopathy with nemaline rods and cap structures caused by a mutation in the beta-tropomyosin gene (TPM2)

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1334-8

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n11:17846275

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17846275

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9

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64

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n13:ARCHNEUR.64.9.1334

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10.1001/ARCHNEUR.64.9.1334