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Article

Severe scoliosis in a patient with COLQ mutation and congenital myasthenic syndrome: a clue for diagnosis.

Acta neurologica Belgica - 1 Dec 2013

Duran Güntülü Sare, Uzunhan Tuğçe Aksu, Ekici Barış, Çıtak Agop, Aydınlı Nur, Çalışkan Mine

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Share to Acetylcholinesterase
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 23371844
DOI: 10.1007/s13760-013-0179-5

Genes

COLQ

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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