X-linked cardioskeletal myopathy and neutropenia (Barth syndrome)-MIM 302060
- PMID: 10484787
- DOI: 10.1016/s0022-3476(99)70118-6
X-linked cardioskeletal myopathy and neutropenia (Barth syndrome)-MIM 302060
Comment on
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Genetic analysis of the G4.5 gene in families with suspected Barth syndrome.J Pediatr. 1999 Sep;135(3):311-5. doi: 10.1016/s0022-3476(99)70126-5. J Pediatr. 1999. PMID: 10484795
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