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Editorial
. 2012 Nov 1;186(9):820-1.
doi: 10.1164/rccm.201209-1666ED.

Waiting in anticipation: the genetics of pulmonary arterial hypertension

Editorial

Waiting in anticipation: the genetics of pulmonary arterial hypertension

Micheala A Aldred et al. Am J Respir Crit Care Med. .
No abstract available

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References

    1. Brook JD, McCurrach ME, Harley HG, Buckler AJ, Church D, Aburatani H, Hunter K, Stanton VP, Thirion JP, Hudson T, et al. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member. Cell 1992;69:385. - PubMed
    1. Harley HG, Rundle SA, MacMillan JC, Myring J, Brook JD, Crow S, Reardon W, Fenton I, Shaw DJ, Harper PS. Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy. Am J Hum Genet 1993;52:1164–1174 - PMC - PubMed
    1. Loyd JE, Butler MG, Foroud TM, Conneally PM, Phillips JA, III, Newman JH. Genetic anticipation and abnormal gender ratio at birth in familial primary pulmonary hypertension. Am J Respir Crit Care Med 1995;152:93–97 - PMC - PubMed
    1. Loyd JE, Slovis B, Phillips JA, III, Butler MG, Foroud TM, Conneally PM, Newman JH. The presence of genetic anticipation suggests that the molecular basis of familial primary pulmonary hypertension may be trinucleotide repeat expansion. Chest 1997;111:82S–83S - PMC - PubMed
    1. Lane KB, Machado RD, Pauciulo M, Thomson JR, Phillips JA, 3rd, Loyd JE, Nichols WC, Trembath RC; The International PPH Consortium Heterozygous germline mutations in BMPR2, encoding a TGF-beta receptor, cause familial primary pulmonary hypertension. Nat Genet 2000;26:81–84 - PubMed

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