MCM3AP in recessive axonal neuropathy and mild intellectual disability

E. Ylikallio; R. Woldegebriel; M. Tumiati; P. Isohanni; M. M. Ryan; Z. Stark; W. Maie; S. L. Sawyer; K. M. Bell; A. Oshlack; P. L. Lockhart; M. Shcherbii; A. Estrada-Cuzcano; D. Atkinson; T. Hartley; M. Tetreault; I. Cuppen; W. L. van der Pol; A. Candayan; E. Battaloglu; Y. Parman; K. L. I. van Gassen; M. H. van den Boogaard; K. M. Boycott; L. Kauppi; A. Jordanova; T. Lonnqvist; H. Tyynismaa

MCM3AP in recessive axonal neuropathy and mild intellectual disability

E. Ylikallio
, R. Woldegebriel
, M. Tumiati
, P. Isohanni
, M. M. Ryan
, Z. Stark
, W. Maie
, S. L. Sawyer
, K. M. Bell
, A. Oshlack
, P. L. Lockhart
, M. Shcherbii
, A. Estrada-Cuzcano
, D. Atkinson
, T. Hartley
, M. Tetreault
, I. Cuppen
, W. L. van der Pol
, A. Candayan
, E. Battaloglu

Y. Parman, K. L. I. van Gassen, M. H. van den Boogaard, K. M. Boycott, L. Kauppi, A. Jordanova, T. Lonnqvist, H. Tyynismaa

Tutkimustuotos: Artikkelijulkaisu › Konferenssiesitelmän abstrakti › vertaisarvioitu

Alkuperäiskieli	englanti
Lehti	European Journal of Human Genetics
Vuosikerta	26
Sivut	40-41
Sivumäärä	2
ISSN	1018-4813
Tila	Julkaistu - 2018
OKM-julkaisutyyppi	Ei sovellu
Tapahtuma	50th European-Society-of-Human-Genetics (ESHG) Conference - Copenhagen, Tanska Kesto: 27 toukok. 2017 → 30 toukok. 2017

Siteeraa tätä

Ylikallio, E., Woldegebriel, R., Tumiati, M., Isohanni, P., Ryan, M. M., Stark, Z., Maie, W., Sawyer, S. L., Bell, K. M., Oshlack, A., Lockhart, P. L., Shcherbii, M., Estrada-Cuzcano, A., Atkinson, D., Hartley, T., Tetreault, M., Cuppen, I., van der Pol, W. L., Candayan, A., ... Tyynismaa, H. (2018). MCM3AP in recessive axonal neuropathy and mild intellectual disability. European Journal of Human Genetics, 26, 40-41.

@article{b21a72ce34d740feb31d94701377a22b,

title = "MCM3AP in recessive axonal neuropathy and mild intellectual disability",

author = "E. Ylikallio and R. Woldegebriel and M. Tumiati and P. Isohanni and Ryan, \{M. M.\} and Z. Stark and W. Maie and Sawyer, \{S. L.\} and Bell, \{K. M.\} and A. Oshlack and Lockhart, \{P. L.\} and M. Shcherbii and A. Estrada-Cuzcano and D. Atkinson and T. Hartley and M. Tetreault and I. Cuppen and \{van der Pol\}, \{W. L.\} and A. Candayan and E. Battaloglu and Y. Parman and \{van Gassen\}, \{K. L. I.\} and \{van den Boogaard\}, \{M. H.\} and Boycott, \{K. M.\} and L. Kauppi and A. Jordanova and T. Lonnqvist and H. Tyynismaa",

year = "2018",

language = "English",

volume = "26",

pages = "40--41",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

publisher = "Springer",

note = "50th European-Society-of-Human-Genetics (ESHG) Conference ; Conference date: 27-05-2017 Through 30-05-2017",

}

Ylikallio, E, Woldegebriel, R, Tumiati, M, Isohanni, P, Ryan, MM, Stark, Z, Maie, W, Sawyer, SL, Bell, KM, Oshlack, A, Lockhart, PL, Shcherbii, M, Estrada-Cuzcano, A, Atkinson, D, Hartley, T, Tetreault, M, Cuppen, I, van der Pol, WL, Candayan, A, Battaloglu, E, Parman, Y, van Gassen, KLI, van den Boogaard, MH, Boycott, KM, Kauppi, L, Jordanova, A, Lonnqvist, T & Tyynismaa, H 2018, 'MCM3AP in recessive axonal neuropathy and mild intellectual disability', European Journal of Human Genetics, Vuosikerta 26, Sivut 40-41.

TY - JOUR

T1 - MCM3AP in recessive axonal neuropathy and mild intellectual disability

AU - Ylikallio, E.

AU - Woldegebriel, R.

AU - Tumiati, M.

AU - Isohanni, P.

AU - Ryan, M. M.

AU - Stark, Z.

AU - Maie, W.

AU - Sawyer, S. L.

AU - Bell, K. M.

AU - Oshlack, A.

AU - Lockhart, P. L.

AU - Shcherbii, M.

AU - Estrada-Cuzcano, A.

AU - Atkinson, D.

AU - Hartley, T.

AU - Tetreault, M.

AU - Cuppen, I.

AU - van der Pol, W. L.

AU - Candayan, A.

AU - Battaloglu, E.

AU - Parman, Y.

AU - van Gassen, K. L. I.

AU - van den Boogaard, M. H.

AU - Boycott, K. M.

AU - Kauppi, L.

AU - Jordanova, A.

AU - Lonnqvist, T.

AU - Tyynismaa, H.

PY - 2018

Y1 - 2018

M3 - Meeting Abstract

SN - 1018-4813

VL - 26

SP - 40

EP - 41

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

T2 - 50th European-Society-of-Human-Genetics (ESHG) Conference

Y2 - 27 May 2017 through 30 May 2017

ER -