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Article

Screening of the LIX1 gene in Japanese and Malaysian patients with SMA and/or SMA-like disorder.

Brain & development - 1 May 2010

Sasongko Teguh Haryo, Gunadi, Yusoff Surini, Atif Amin Baig, Fatemeh Hayati, Rani Abdulqawee, Marini Marzuki, Ab Aziz Che Badariah, Zabidi-Hussin Z A M H, Nishio Hisahide, Zilfalil Bin Alwi

Abstract excerpt

BACKGROUND: The majority of spinal muscular atrophy (SMA) patients showed homozygous deletion or other mutations of SMN1. However, the genetic etiology of a significant number of SMA patients has not been clarified. Recently, mutation in the gene underlying cat SMA, limb expression 1 (LIX1), has...

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Source

Identifiers

PMID: 19664890
DOI: 10.1016/j.braindev.2009.06.008

Genes

LIX1
SMN1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19664890-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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