Comprehensive clinical, biochemical, radiological and genetic analysis of 28 Turkish cases with suspected metachromatic leukodystrophy and their relatives-Reference-Cited by-同舟云学术

Comprehensive clinical, biochemical, radiological and genetic analysis of 28 Turkish cases with suspected metachromatic leukodystrophy and their relatives

Published:2020-12 Issue: Volume:25 Page:100688
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

Pekgül Faruk,Eroğlu-Ertuğrul Nesibe Gevher,Bekircan-Kurt Can Ebru,Erdem-Ozdamar Sevim,Çetinkaya Arda,Tan Ersin,Konuşkan Bahadır,Karaağaoğlu Ergun,Topçu Meral,Akarsu Nurten Ayşe,Oguz Kader K.,Anlar Banu,Özkara Hatice Asuman

Funder

Hacettepe University Scientific Research Coordination Unit

Hacettepe University

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference41 articles.

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5. Multiple sulfatase deficiency and the nature of the sulfatase family;Hopwood,2014

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