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2014 | 1 |
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Spondylometaphyseal dysplasia with cone-rod dystrophy.
Am J Med Genet A. 2004 Sep 1;129A(3):265-76. doi: 10.1002/ajmg.a.30145.
Am J Med Genet A. 2004.
PMID: 15326626
Mutations in PCYT1A, encoding a key regulator of phosphatidylcholine metabolism, cause spondylometaphyseal dysplasia with cone-rod dystrophy.
Hoover-Fong J, Sobreira N, Jurgens J, Modaff P, Blout C, Moser A, Kim OH, Cho TJ, Cho SY, Kim SJ, Jin DK, Kitoh H, Park WY, Ling H, Hetrick KN, Doheny KF, Valle D, Pauli RM.
Hoover-Fong J, et al.
Am J Hum Genet. 2014 Jan 2;94(1):105-12. doi: 10.1016/j.ajhg.2013.11.018.
Am J Hum Genet. 2014.
PMID: 24387990
Free PMC article.
No abstract available.
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