Carrier frequency of SMA by quantitative analysis of the SMN1 deletion in the Iranian population

Autor: Hasanzad, M, Azad, M, Kahrizi, K, Saffar, BS, Nafisi, S, Keyhanidoust, Z, Azimian, M, Refah, AA, Also, E, Urtizberea, JA, Tizzano, EF, Najmabadi, H

Publikováno v: EUROPEAN JOURNAL OF NEUROLOGY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
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Background and purpose: Spinal muscular atrophy (SMA) is a common autosomal recessive neuromuscular disorder. Carrier frequency studies of SMA have been reported for various populations. Although no large-scale population-based studies of SMA have be

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Carrier frequency of SMA by quantitative analysis of the SMN1 deletion in the Iranian population.

Autor: Hasanzad M; Genetics Research Center, University of Social Welfare & Rehabilitation Sciences, Tehran, Iran., Azad M, Kahrizi K, Saffar BS, Nafisi S, Keyhanidoust Z, Azimian M, Refah AA, Also E, Urtizberea JA, Tizzano EF, Najmabadi H

Publikováno v: European journal of neurology [Eur J Neurol] 2010 Jan; Vol. 17 (1), pp. 160-2. Date of Electronic Publication: 2009 Jun 15.