Mutations in MYO1H cause a recessive form of central hypoventilation with autonomic dysfunction. (Q47810860)
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scientific article published on 4 August 2017
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Mutations in MYO1H cause a recessive form of central hypoventilation with autonomic dysfunction. |
scientific article published on 4 August 2017 |
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Mutations in MYO1H cause a recessive form of central hypoventilation with autonomic dysfunction. (English)
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Stefan Mundlos
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Carmen Birchmeier
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Debra E Weese-Mayer
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Izabela Harabula
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Norma Leonard
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4 August 2017
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54
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11
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754-761
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Identifiers
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