Neuroimaging features of MOPDII in ten patients with PCNT mutation: A Tertiary Centre Experience

Akcahan Akalin; Rahsan Gocmen; Pelin Simsek-Kiper; Ekim Taskiran; Yasemin Alanay; Vildan Goknur Haliloglu; Gulen Eda Utine; Koray Boduroglu

Neuroimaging features of MOPDII in ten patients with PCNT mutation: A Tertiary Centre Experience

Akcahan Akalin
, Rahsan Gocmen
, Pelin Simsek-Kiper
, Ekim Taskiran
, Yasemin Alanay
, Vildan Goknur Haliloglu
, Gulen Eda Utine
, Koray Boduroglu

Hacettepe University
Acibadem MAA University
Med Fac

Research output: Contribution to journal › Meeting Abstract › peer-review

Original language	English
Pages (from-to)	408-409
Number of pages	2
Journal	European Journal of Human Genetics
Volume	32
Publication status	Published - Jan 2024
Event	56th Annual Conference of the European-Society-of-Human-Genetics (ESHG) - Glasgow Duration: 10 Jun 2023 → 13 Jun 2023

Cite this

@article{8ce05f5db95b43b48ea7d64bec95d5ef,

title = "Neuroimaging features of MOPDII in ten patients with PCNT mutation: A Tertiary Centre Experience",

author = "Akcahan Akalin and Rahsan Gocmen and Pelin Simsek-Kiper and Ekim Taskiran and Yasemin Alanay and Haliloglu, \{Vildan Goknur\} and Utine, \{Gulen Eda\} and Koray Boduroglu",

year = "2024",

month = jan,

language = "English",

volume = "32",

pages = "408--409",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

publisher = "Springer Nature",

note = "56th Annual Conference of the European-Society-of-Human-Genetics (ESHG) ; Conference date: 10-06-2023 Through 13-06-2023",

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TY - JOUR

T1 - Neuroimaging features of MOPDII in ten patients with PCNT mutation

T2 - 56th Annual Conference of the European-Society-of-Human-Genetics (ESHG)

AU - Akalin, Akcahan

AU - Gocmen, Rahsan

AU - Simsek-Kiper, Pelin

AU - Taskiran, Ekim

AU - Alanay, Yasemin

AU - Haliloglu, Vildan Goknur

AU - Utine, Gulen Eda

AU - Boduroglu, Koray

PY - 2024/1

Y1 - 2024/1

UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=performanshacettepe&SrcAuth=WosAPI&KeyUT=WOS:001147414902163&DestLinkType=FullRecord&DestApp=WOS_CPL

M3 - Meeting Abstract

SN - 1018-4813

VL - 32

SP - 408

EP - 409

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

Y2 - 10 June 2023 through 13 June 2023

ER -

Neuroimaging features of MOPDII in ten patients with PCNT mutation: A Tertiary Centre Experience

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