The face of lysosomal storage disorders in India: a need for early diagnosis.

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The face of lysosomal storage disorders in India: a need for early diagnosis.

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2014 nî lūn-bûn

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2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

2014年论文

@zh

2014年论文

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The face of lysosomal storage disorders in India: a need for early diagnosis.

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The face of lysosomal storage disorders in India: a need for early diagnosis.

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The face of lysosomal storage disorders in India: a need for early diagnosis.

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P1476

The face of lysosomal storage disorders in India: a need for early diagnosis.

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P2093

Keya Lahiri

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Mamta Muranjan

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Nirmal Solanki

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Shruti Agarwal

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P2860

Novel mutations in the glucocerebrosidase gene of Indian patients with Gaucher disease.

A reappraisal of Gaucher disease-diagnosis and disease management algorithms.

Lysosomal storage disorders: the need for better pediatric recognition and comprehensive care.

Fabry disease in childhood.

The mucopolysaccharidoses: a heterogeneous group of disorders with variable pediatric presentations.

Pompe disease in infants and children.

A study on the nature of genetic metabolic practice at a major paediatric referral centre.

Rapidly rising rates of overweight and obesity coupled with persistently high rates of undernutrition among school aged children in an urban Indo-Asian population: authors' response.

Burden of genetic disorders in India.

Spectrum of Lysosomal storage disorders at a medical genetics center in northern India.

P2888

s12098-014-1628-8

P304

525-529

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scholarly article

P356

10.1007/S12098-014-1628-8

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P433

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P478

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P577

2014-12-09T00:00:00Z

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P698

25482214

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P921

India