TY - JOUR
T1 - Erratum
T2 - Mutations in PRDM5 in Brittle Cornea syndrome identify a pathway regulating extracellular matrix development and maintenance (American Journal of Human Genetics (2011) 88 (767-777))
AU - Burkitt Wright, Emma M.M.
AU - Spencer, Helen L.
AU - Daly, Sarah B.
AU - Manson, Forbes D.C.
AU - Zeef, Leo A.H.
AU - Urquhart, Jill
AU - Zoppi, Nicoletta
AU - Tosounidis, Ioannis
AU - Mohan, Meyyammai
AU - Madden, Colm
AU - Dodds, Annabel
AU - Chandler, Kate E.
AU - Banka, Siddharth
AU - Au, Leon
AU - Clayton-Smith, Jill
AU - Khan, Naz
AU - Biesecker, Leslie G.
AU - Wilson, Meredith
AU - Rohrbach, Marianne
AU - Colombi, Marina
AU - Giunta, Cecilia
AU - Black, Graeme C.M.
PY - 2011/8/12
Y1 - 2011/8/12
N2 - (American Journal of Human Genetics 88, 767–777; June 10, 2011).In the original version of this paper, there was a misalignment of numbering of individuals of family BCS-001 in Table 1, affecting individuals IV:7 (unaffected), IV:8 (heterozygous), and IV:10 (homozygous). The corrected table appears below. The authors regret the error.
AB - (American Journal of Human Genetics 88, 767–777; June 10, 2011).In the original version of this paper, there was a misalignment of numbering of individuals of family BCS-001 in Table 1, affecting individuals IV:7 (unaffected), IV:8 (heterozygous), and IV:10 (homozygous). The corrected table appears below. The authors regret the error.
UR - http://www.scopus.com/inward/record.url?scp=80051654720&partnerID=8YFLogxK
U2 - 10.1016/j.ajhg.2011.07.013
DO - 10.1016/j.ajhg.2011.07.013
M3 - Commentary/debate
AN - SCOPUS:80051654720
SN - 0002-9297
VL - 89
SP - 346
JO - American Journal of Human Genetics
JF - American Journal of Human Genetics
IS - 2
ER -