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Review

. 1999 Sep;135(3):273-6.

doi: 10.1016/s0022-3476(99)70118-6.

X-linked cardioskeletal myopathy and neutropenia (Barth syndrome)-MIM 302060

P G Barth, R J Wanders, P Vreken

PMID: 10484787
DOI: 10.1016/s0022-3476(99)70118-6

Review

X-linked cardioskeletal myopathy and neutropenia (Barth syndrome)-MIM 302060

P G Barth et al. J Pediatr. 1999 Sep.

. 1999 Sep;135(3):273-6.

doi: 10.1016/s0022-3476(99)70118-6.

Authors

P G Barth, R J Wanders, P Vreken

PMID: 10484787
DOI: 10.1016/s0022-3476(99)70118-6

No abstract available

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Comment on

Genetic analysis of the G4.5 gene in families with suspected Barth syndrome.
Cantlay AM, Shokrollahi K, Allen JT, Lunt PW, Newbury-Ecob RA, Steward CG. Cantlay AM, et al. 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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