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PubMed (OMIM) for id: 9987
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229th ENMC international workshop: Limb girdle muscular dystrophies - Nomenclature and reformed classification Naarden, the Netherlands, 17-19 March 2017.
Neuromuscul Disord. 2018 Aug;28(8):702-710. doi: 10.1016/j.nmd.2018.05.007. Epub 2018 May 24.
Neuromuscul Disord. 2018.
PMID: 30055862
No abstract available.
A defect in the RNA-processing protein HNRPDL causes limb-girdle muscular dystrophy 1G (LGMD1G).
Vieira NM, Naslavsky MS, Licinio L, Kok F, Schlesinger D, Vainzof M, Sanchez N, Kitajima JP, Gal L, Cavaçana N, Serafini PR, Chuartzman S, Vasquez C, Mimbacas A, Nigro V, Pavanello RC, Schuldiner M, Kunkel LM, Zatz M.
Vieira NM, et al.
Hum Mol Genet. 2014 Aug 1;23(15):4103-10. doi: 10.1093/hmg/ddu127. Epub 2014 Mar 18.
Hum Mol Genet. 2014.
PMID: 24647604
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A new form of autosomal dominant limb-girdle muscular dystrophy (LGMD1G) with progressive fingers and toes flexion limitation maps to chromosome 4p21.
Starling A, Kok F, Passos-Bueno MR, Vainzof M, Zatz M.
Starling A, et al.
Eur J Hum Genet. 2004 Dec;12(12):1033-40. doi: 10.1038/sj.ejhg.5201289.
Eur J Hum Genet. 2004.
PMID: 15367920
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Two forms of expression and genomic structure of the human heterogeneous nuclear ribonucleoprotein D-like JKTBP gene (HNRPDL).
Kamei D, Tsuchiya N, Yamazaki M, Meguro H, Yamada M.
Kamei D, et al.
Gene. 1999 Mar 4;228(1-2):13-22. doi: 10.1016/s0378-1119(99)00020-7.
Gene. 1999.
PMID: 10072754
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Cloning and characterization of a cDNA encoding a novel heterogeneous nuclear ribonucleoprotein-like protein and its expression in myeloid leukemia cells.
Tsuchiya N, Kamei D, Takano A, Matsui T, Yamada M.
Tsuchiya N, et al.
J Biochem. 1998 Mar;123(3):499-507. doi: 10.1093/oxfordjournals.jbchem.a021964.
J Biochem. 1998.
PMID: 9538234
Free article.
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Molecular cloning of the cDNA encoding A + U-rich element RNA binding factor.
Doi A, Shiosaka T, Takaoka Y, Yanagisawa K, Fujita S.
Doi A, et al.
Biochim Biophys Acta. 1998 Mar 4;1396(1):51-6. doi: 10.1016/s0167-4781(97)00223-6.
Biochim Biophys Acta. 1998.
PMID: 9524220
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