TY - JOUR
T1 - Erratum
T2 - Mutations in MAPKBP1 Cause Juvenile or Late-Onset Cilia-Independent Nephronophthisis (American Journal of Human Genetics (2017) 100(2) (323–333)(S0002929716305353)(10.1016/j.ajhg.2016.12.011))
AU - Macia, Maxence S.
AU - Halbritter, Jan
AU - Delous, Marion
AU - Bredrup, Cecilie
AU - Gutter, Arthur
AU - Filhol, Emilie
AU - Mellgren, Anne E.C.
AU - Leh, Sabine
AU - Bizet, Albane
AU - Braun, Daniela A.
AU - Gee, Heon Y.
AU - Silbermann, Flora
AU - Henry, Charline
AU - Krug, Pauline
AU - Bole-Feysot, Christine
AU - Nitschké, Patrick
AU - Joly, Dominique
AU - Nicoud, Philippe
AU - Paget, André
AU - Haugland, Heidi
AU - Brackmann, Damien
AU - Ahmet, Nayir
AU - Sandford, Richard
AU - Cengiz, Nurcan
AU - Knappskog, Per M.
AU - Boman, Helge
AU - Linghu, Bolan
AU - Yang, Fan
AU - Oakeley, Edward J.
AU - Saint Mézard, Pierre
AU - Sailer, Andreas W.
AU - Johansson, Stefan
AU - Rødahl, Eyvind
AU - Saunier, Sophie
AU - Hildebrandt, Friedhelm
AU - Benmerah, Alexandre
N1 - Publisher Copyright:
© 2017
PY - 2017/2/2
Y1 - 2017/2/2
N2 - (The American Journal of Human Genetics 100, 323–333; February 2, 2017) In the version of this paper published online on January 12, there were three errors. First, on page 2, the mutation in NPH2139-22 is described as “…(c.1318C>T [p.Arg544Gln]) never reported in ExAC database…” but in Table 1 (row 4, column 3), the mutation is designated c.1631G>A. The nomenclature c.1631G>A (in Table 1) is correct. Second, on page 3, the text says “…in-frame deletion of 39 amino acids (aa 396 to 435)…” but in Table 1 and Figure 1, the range is given as p.396_445del. Again, the nomenclature in Table 1 and Figure 1 is correct and the text on page 3 should have been “…in-frame deletion of 49 amino acids (aa 396 to 445)…” Third, in Table 1, the fifth column entries for rows 1 and 2 should both read “7, 32 Het.” All three of these errors have been corrected in the version of the paper printed and currently online. The authors apologize for these errors.
AB - (The American Journal of Human Genetics 100, 323–333; February 2, 2017) In the version of this paper published online on January 12, there were three errors. First, on page 2, the mutation in NPH2139-22 is described as “…(c.1318C>T [p.Arg544Gln]) never reported in ExAC database…” but in Table 1 (row 4, column 3), the mutation is designated c.1631G>A. The nomenclature c.1631G>A (in Table 1) is correct. Second, on page 3, the text says “…in-frame deletion of 39 amino acids (aa 396 to 435)…” but in Table 1 and Figure 1, the range is given as p.396_445del. Again, the nomenclature in Table 1 and Figure 1 is correct and the text on page 3 should have been “…in-frame deletion of 49 amino acids (aa 396 to 445)…” Third, in Table 1, the fifth column entries for rows 1 and 2 should both read “7, 32 Het.” All three of these errors have been corrected in the version of the paper printed and currently online. The authors apologize for these errors.
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U2 - 10.1016/j.ajhg.2017.01.025
DO - 10.1016/j.ajhg.2017.01.025
M3 - Comment/debate
C2 - 28157543
AN - SCOPUS:85011818964
SN - 0002-9297
VL - 100
SP - 372
JO - American Journal of Human Genetics
JF - American Journal of Human Genetics
IS - 2
ER -